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(2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-carboxylate

Base Information Edit
  • Chemical Name:(2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-carboxylate
  • CAS No.:171192-72-6
  • Molecular Formula:C14H19NO3
  • Molecular Weight:249.31
  • Hs Code.:
  • Mol file:171192-72-6.mol
(2R,4R)-ethyl N<sup>1</sup>-benzyl-4-hydroxypyrrolidine-2-carboxylate

Synonyms:(2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-carboxylate

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Chemical Property of (2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-carboxylate Edit
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Technology Process of (2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-carboxylate

There total 13 articles about (2R,4R)-ethyl N1-benzyl-4-hydroxypyrrolidine-2-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:
(2R,4R)-2-ethoxycarbonyl-4-hydroxypyrrolidine hydrochloride; benzyl bromide; With triethylamine; In chloroform; for 6h; Heating;
With sodium hydroxide; In chloroform; at 20 ℃;
DOI:10.1016/j.tetasy.2003.08.019
Guidance literature:
(S)-ethyl 2-(benzyl(oxiran-2-ylmethyl)amino)acetate; With lithium hexamethyldisilazane; In tetrahydrofuran; at -60 - -15 ℃; for 0.166667h;
With magnesium bromide ethyl etherate; In tetrahydrofuran; at -60 - 25 ℃; for 3.5h; Reagent/catalyst; diastereoselective reaction;
DOI:10.1016/j.tetlet.2015.03.119
Guidance literature:
With lithium hexamethyldisilazane; In N,N-dimethyl-formamide; at -58 - 50 ℃; for 4.66667h; diastereoselective reaction;
DOI:10.1016/j.tetlet.2015.03.119
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