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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367486Generated: October 25, 2026

Water → (1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxymethyl-cyclopentanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1367486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-cyclopentane-1,2-dicarboxylic acid monoethyl esterHCID 59619299—
SolventTetrahydrofuranHCID 8028—
Product(1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxymethyl-cyclopentanecarboxylic acid ethyl esterHCID 5961945173.2%

Reaction Steps

To a cold (ice bath) solution of (1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-cyclopentane-1,2-dicarboxylic acid monoethyl ester (epimeric mixture, 0.7 g) in tetrahydrofuran (3.5 mL) was slowly added a borane complex with tetrahydrofuran (1M, 2.7 mL). The resulting solution was stirred for 3 h in the ice bath then slowly poured into water. The mixture was extracted with diethylether. The combined organic layers were washed with brine and dried over sodium sulfate then concentrated in vacuo. The residue was purified by flash chromatography on silica gel with cyclohexane/ethylacetate (6:1 v/v) as eluant to afford the title compound (0.49 g, 73%) as light yellow oil. MS (EI): 303.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-ff4d2bb326124cd0ad71cd2a15c4d7ba
Source noteuspto-grants-2011_02