Brief introduction of (R)-tert-Butyl piperidin-3-ylcarbamate

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.309956-78-3. In my other articles, you can also check out more blogs about 309956-78-3

Application of 309956-78-3, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 309956-78-3, name is (R)-tert-Butyl piperidin-3-ylcarbamate. In an article，Which mentioned a new discovery about 309956-78-3

The invention relates to a synthesis method of chiral aminopiperidine and derivatives thereof. 3 . The invention is carried out by R (or S) – piperidine -3 – ethyl ester – L (or D) – L (or D)-tartrate after benzyl protection followed by azide and Curtitius rearrangement to R or S -benzyl -3 -aminopiperidine. R or S – benzyl -3 – aminopiperidine undergoes debenzylation to give R or S -amino piperidine, R or S – benzyl -3 – aminopiperidine through 3 -t-butoxycarbonyl protection, for example. Of R or S – (3 – t-butoxycarbonyl amino) piperidine, R or S – (3 – t-butoxycarbonyl amino) piperidine under acidic conditions can give R or S – 3-aminopiperidine, corresponding salts. The synthesis method provides a low-cost, easily-industrialized chiral 3 -aminopiperidine with high optical purity and a method. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.309956-78-3. In my other articles, you can also check out more blogs about 309956-78-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H13394N – PubChem