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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374304Generated: November 1, 2026

benzyl (S)-1-((1S,2S,4R)-4-(tert-butyldimethylsilyloxy)-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate → benzyl (S)-1-((1S,2S,4R)-4-hydroxy-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1374304

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (S)-1-((1S,2S,4R)-4-(tert-butyldimethylsilyloxy)-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamateHCID 86596870—
SolventAcOH THF waterHCID 21877175—
Productbenzyl (S)-1-((1S,2S,4R)-4-hydroxy-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamateHCID 8659686997.9%

Reaction Steps

Benzyl (S)-1-((1S,2S,4R)-4-(tert-butyldimethylsilyloxy)-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate (1.0 g) was dissolved in a 4/1/1 mixture of AcOH/THF/H2O (60 mL). After 72 h, additional 4/1/1 mixture of AcOH/THF/H2O (30 mL) was added. This solution was stirred an additional 24 h before it was concentrated. The residue was dissolved in EtOAc and washed with saturated NaHCO3, dried (MgSO4), filtered, and concentrated in vacuo to afford benzyl (S)-1-((1S,2S,4R)-4-hydroxy-2-isopropylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate (750 mg). MS found: (M+H)+=375.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-53b20c646a5a46158b2bee974ff27d78
Source noteuspto-grants-2007_01