Category: 26458-78-6

A new synthetic route of Quinuclidine-4-carbonitrile

The chemical industry reduces the impact on the environment during synthesis, 26458-78-6, , I believe this compound will play a more active role in future production and life.

26458-78-6, A common heterocyclic compound, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.”26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

The chemical industry reduces the impact on the environment during synthesis, 26458-78-6, , I believe this compound will play a more active role in future production and life.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

A new synthetic route of 26458-78-6

The chemical industry reduces the impact on the environment during synthesis, 26458-78-6, , I believe this compound will play a more active role in future production and life.

26458-78-6, A common heterocyclic compound, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.”26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

The chemical industry reduces the impact on the environment during synthesis, 26458-78-6, , I believe this compound will play a more active role in future production and life.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

Some scientific research about Quinuclidine-4-carbonitrile

The chemical industry reduces the impact on the environment during synthesis, Quinuclidine-4-carbonitrile, , I believe this compound will play a more active role in future production and life.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact.26458-78-6, Quinuclidine-4-carbonitrile it is a common compound, a new synthetic route is introduced below.26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

The chemical industry reduces the impact on the environment during synthesis, Quinuclidine-4-carbonitrile, , I believe this compound will play a more active role in future production and life.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

The important role of 26458-78-6

The chemical industry reduces the impact on the environment during synthesis,26458-78-6,Quinuclidine-4-carbonitrile,I believe this compound will play a more active role in future production and life.

26458-78-6, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Quinuclidine-4-carbonitrile, cas is 26458-78-6,the quinuclidine compound, it is a common compound, a new synthetic route is introduced below.

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

The chemical industry reduces the impact on the environment during synthesis,26458-78-6,Quinuclidine-4-carbonitrile,I believe this compound will play a more active role in future production and life.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

The origin of a common compound about Quinuclidine-4-carbonitrile

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

A common heterocyclic compound, 26458-78-6,Quinuclidine-4-carbonitrile, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route. 26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

A new synthetic route of Quinuclidine-4-carbonitrile

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

A common heterocyclic compound, 26458-78-6,Quinuclidine-4-carbonitrile, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route. 26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

The origin of a common compound about 26458-78-6

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

A common heterocyclic compound, 26458-78-6,Quinuclidine-4-carbonitrile, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route. 26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

A new synthetic route of Quinuclidine-4-carbonitrile

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

A common heterocyclic compound, 26458-78-6,Quinuclidine-4-carbonitrile, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route. 26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

This compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,26458-78-6,Quinuclidine-4-carbonitrile,its application will become more common.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

The important role of 26458-78-6

With the complex challenges of chemical substances, we look forward to future research findings about Quinuclidine-4-carbonitrile

Name is Quinuclidine-4-carbonitrile, as a common heterocyclic compound, it belongs to quinuclidine compound, and cas is 26458-78-6, its synthesis route is as follows.,26458-78-6

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

With the complex challenges of chemical substances, we look forward to future research findings about Quinuclidine-4-carbonitrile

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider

Application of Quinuclidine-4-carbonitrile

Big data shows that 26458-78-6 is playing an increasingly important role.

Quinuclidine-4-carbonitrile,26458-78-6,belong quinuclidine compound,the synthetic route is as follows.

Quinuclidine-4-carbonitrile (4 g, 29.4 mmol) was treated with 30 mL of 6 N aqueous HCl solution and stirred under reflux for 16 hr. The reaction mixture was cooled and evaporated to dryness under reduced pressure. The solid obtained was triturated with 20% ether-hexane to afford the HCl salt of quinuclidine-4-carboxylic acid (5.5 g, quantitative).

Big data shows that 26458-78-6 is playing an increasingly important role.

Reference£º
Patent; CoMentis, Inc.; BILCER, Geoffrey M.; NG, Raymond; (104 pag.)US2016/9706; (2016); A1;,
Quinuclidine – Wikipedia
Quinuclidine | C7H13N | ChemSpider