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

Base Information

Chemical Name:(3S, 5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:287476-38-4
Molecular Formula:C₂₃H₃₇NO₅Si
Molecular Weight:435.636
Hs Code.:

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

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

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

There total 4 articles about (3S, 5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-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: 100.0%

: 270262-17-4
(5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-3-(4-methoxyphenyl)-2-oxo-2,5-dihydropyrrole-1-carboxylic acid tert-butyl ester

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

Guidance literature:: With hydrogen; 20percent Pd(OH)2/C; In ethanol; under 2280.15 Torr;
DOI:10.1021/jm0001368

Reference yield:

: 5720-07-0
4-methoxyphenylboronic acid

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

Guidance literature:: Multi-step reaction with 2 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

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

Reference yield:

: 126587-41-5
tert-butyl (2R)-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate

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

Guidance literature:: Multi-step reaction with 3 steps

1: 31 percent / I₂; pyridine / CCl₄

2: 77 percent / Pd(PPh₃)4; aq. Na₂CO₃ / toluene / 1 h / Heating

3: 100 percent / H₂ / 20percent Pd(OH)2/C / ethanol / 2280.15 Torr

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