(R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Name:(R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:1314325-36-4
Molecular Formula:C₁₆H₂₆N₂O₃
Molecular Weight:294.394
Hs Code.:

Synonyms:(R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

There total 1 articles about (R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 56.0%

: 1314325-35-3
1-(5-bromo-1,2,3,4-tetrahydropyridin-1-yl)ethan-1-one

: 86953-79-9
tert-butyl pyrrolidine-1-carboxylate

: 1314325-36-4
(R)-2-(1-acetyl-1,4,5,6-tetrahydropyridin-3-yl)pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: tert-butyl pyrrolidine-1-carboxylate; With C₁₃H₂₆N₂; sec.-butyllithium; (-)-sparteine; In hexane; tert-butyl methyl ether; at -78 ℃; for 1.5h; Inert atmosphere;

With zinc(II) chloride; In diethyl ether; hexane; tert-butyl methyl ether; at -78 - 20 ℃; Inert atmosphere;

1-(5-bromo-1,2,3,4-tetrahydropyridin-1-yl)ethan-1-one; With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tri tert-butylphosphoniumtetrafluoroborate; In diethyl ether; hexane; tert-butyl methyl ether; at 20 ℃; for 72h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jo2011347