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tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate

Base Information Edit
  • Chemical Name:tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate
  • CAS No.:1350627-37-0
  • Molecular Formula:C12H23NO3
  • Molecular Weight:229.32
  • Hs Code.:
  • Mol file:1350627-37-0.mol
tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate

Synonyms:tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate

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Chemical Property of tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate Edit
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Technology Process of tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate

There total 1 articles about tert-butyl (2S)-2-[(2'R)-2'-hydroxypropyl]pyrrolidine-1-carboxylate 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:
Guidance literature:
tert-butyl pyrrolidine-1-carboxylate; With sec.-butyllithium; (1R,5S,11aS)-3-methyldecahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocine; In diethyl ether; cyclohexane; at -78 ℃; for 4h; Inert atmosphere;
(R)-propylene oxide; With boron trifluoride diethyl etherate; In diethyl ether; cyclohexane; at -78 - 0 ℃; for 3.08333h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/jo4017343
Guidance literature:
Multi-step reaction with 2 steps
1.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
1.2: 0 - 20 °C
2.1: dmap; pyridine / dichloromethane / 0 - 20 °C
With pyridine; dmap; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/acs.jnatprod.0c00871
upstream raw materials:

tert-butyl pyrrolidine-1-carboxylate

(R)-propylene oxide

Downstream raw materials:

(4S,6R)-conioidine A

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