(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Name:(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:270262-20-9
Molecular Formula:C₁₇H₂₃NO₅
Molecular Weight:321.373
Hs Code.:

Synonyms:(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

There total 6 articles about (3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-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: 48.0%

: 287476-38-4
(3S, 5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

: 270262-20-9
(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With hydrogenchloride; In tetrahydrofuran;
DOI:10.1021/jm0001368

Reference yield: 48.0%

: 270262-20-9
(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:

Reference yield:

: 5720-07-0
4-methoxyphenylboronic acid

: 270262-20-9
(3S, 5R)-5-hydroxymethyl-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / Pd(PPh₃)4; aq. Na₂CO₃ / toluene / 1 h / Heating

2: 100 percent / H₂ / 20percent Pd(OH)2/C / ethanol / 2280.15 Torr

3: 48 percent / 0.5 M aq. HCl / tetrahydrofuran

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen; sodium carbonate; 20percent Pd(OH)2/C; In tetrahydrofuran; ethanol; toluene; 1: Suzuki coupling / 2: Catalytic hydrogenation / 3: desilylation;
DOI:10.1021/jm0001368