(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

Base Information

Chemical Name:(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester
CAS No.:1050392-82-9
Molecular Formula:C₁₆H₂₂FNO₃
Molecular Weight:295.354
Hs Code.:

Synonyms:(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

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Chemical Property of (2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

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Technology Process of (2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

There total 5 articles about (2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-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:

: 68766-96-1
ethyl (R)-2-pyrrolidone-5-carboxylate

: 1050392-82-9
(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / dmap / tetrahydrofuran / 5 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: tetrahydrofuran / 1 h / -40 °C

3.1: hydrogenchloride / ethyl acetate / 2 h / 20 °C

3.2: 20 h / 20 °C

4.1: triethylamine / N,N-dimethyl-formamide / 13 h / 20 °C

5.1: lithium borohydride / acetic acid / 14.5 h / 0 - 20 °C

With hydrogenchloride; lithium borohydride; triethylamine; dmap; In tetrahydrofuran; acetic acid; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1050392-46-5
(2R,5S)-5-(4-fluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester

: 1050392-82-9
(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

Guidance literature:: (2R,5S)-5-(4-fluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester; With lithium borohydride; In acetic acid; at 0 - 20 ℃; for 14.5h;

With water; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1050392-82-9
(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / N,N-dimethyl-formamide / 13 h / 20 °C

2: lithium borohydride / acetic acid / 14.5 h / 0 - 20 °C

With lithium borohydride; triethylamine; In acetic acid; N,N-dimethyl-formamide;