2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester
CAS No.:865436-07-3
Molecular Formula:C₁₉H₂₇NO₆
Molecular Weight:365.426
Hs Code.:

Synonyms:2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

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Chemical Property of 2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

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Technology Process of 2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

There total 3 articles about 2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl 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: 85.0%

: 865436-06-2
2S,4R-4-tert-butoxycarbonylmethoxypyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

: 865436-07-3
2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: With sodium tetrahydroborate; lithium chloride; In tetrahydrofuran; ethanol; at 0 - 10 ℃;
DOI:10.1021/jm070002v

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 865436-07-3
2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH; n-Bu₄NI / tetrahydrofuran

1.2: 65 percent / tetrahydrofuran

2.1: 85 percent / LiCl; NaBH₄ / tetrahydrofuran; ethanol / 0 - 10 °C

With sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; sodium hydride; lithium chloride; In tetrahydrofuran; ethanol;
DOI:10.1021/jm070002v

Reference yield:

: 64187-48-0
methyl (2S,4R)-1-benzyloxycarbonyl-4-hydroxypyrrolidine-2-carboxylate

: 865436-07-3
2S,4R-4-tert-butoxycarbonylmethoxy-2-hydroxymethylpyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH; n-Bu₄NI / tetrahydrofuran

1.2: 65 percent / tetrahydrofuran

2.1: 85 percent / LiCl; NaBH₄ / tetrahydrofuran; ethanol / 0 - 10 °C

With sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; sodium hydride; lithium chloride; In tetrahydrofuran; ethanol;
DOI:10.1021/jm070002v