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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953043Generated: November 3, 2026

HCID 10765247, compound → HCID 10646553, compound

https://huagongshe.com/reaction/1953043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10765247HCID 10765247—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 10646553HCID 10646553—

Reaction Steps

A solution of (5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-3-(4-methoxyphenyl)-2-oxo-2,5-dihydropyrrole-1-carboxylic acid tert-butyl ester (1.7 grams, 3.9 mmol) in ethanol (100 mL) was treated with palladium black (300 mg) and hydrogenated in a Parr™ shaker at 3 atmospheres pressure overnight. The catalyst was removed by filtration and the solvent was evaporated to provide crude (3S, 5R)-5-(tert-butyl-dimethylsilanyloxymethyl)-3-(4-methoxyphenyl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester as an oil. This was dissolved in tetrahydrofuran (40 mL) and treated with aqueous 0.5M hydrochloric acid solution (7.2 mL). The resulting mixture was stirred at room temperature overnight, quenched with saturated sodium carbonate solution and extracted twice with methylene chloride. The combined organic extracts were dried over magnesium sulfate and concentrated to an oil. The title compound (551 mg, 48%) was isolated by flash chromatography on silica gel eluting with 20% hexane in ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114361
Source datasetuspto-grants-2000_09
ORD IDord-2bbbafad623d4d5ba8aad95e6b45823f
Source noteuspto-grants-2000_09