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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39614Generated: October 29, 2026

Ethyl Acetate → HCID 86677384, compound

https://huagongshe.com/reaction/39614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant((1S,2S,3R,4R)-2-(3-hydroxybenzyl)-4-(tert-butyldimethylsilyoxy)-3-((S)-3-(tert-butyldimethylsilyoxy)octyl)cyclopentyl)methyl 4-methylbenzenesulfonateHCID 86677385—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86677384HCID 8667738487%

Reaction Conditions

Temperature10 °C

Reaction Steps

A degassed solution of ((1S,2S,3R,4R)-2-(3-hydroxybenzyl)-4-(tert-butyldimethylsilyoxy)-3-((S)-3-(tert-butyldimethylsilyoxy)octyl)cyclopentyl)methyl 4-methylbenzenesulfonate (12.4 g, 0.017 mol) in anhydrous THF (250 ml) at 0° C. under nitrogen was treated with 60% sodium hydride (2.04 g, 0.051 mol). The resulting suspension was stirred for 4 hr at reflux. The reaction was then cooled to 10° C., diluted with ice cold brine (250 ml) and ethyl acetate (500 ml). The reaction mixture was phase separated and the aqueous layer was extracted with ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The solid was filtered off. The solvent was evaporated off under vacuum. The crude product was purified by chromatography on silica gel using a mixture of hexane and ethyl acetate as a gradient eluent. Yield: 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524939B2
Source datasetuspto-grants-2013_09
ORD IDord-ca05604a24cd46f498293eca1f9e682b
Source noteuspto-grants-2013_09