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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367139Generated: November 3, 2026

Benzyl acetate → HCID 57974088, compound

https://huagongshe.com/reaction/1367139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl acetateHCID 8785—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57974029HCID 57974029—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57974088HCID 57974088—

Reaction Steps

To a 0° C. solution of (5R)-5-(3,5-difluorophenyl)thiomorpholin-3-one (247 mg, 1.08 mmol, prepared by analogy to Intermediate 2) in THF (8.0 mL) was added sodium hydride (38 mg, 1.5 mmol, 95% by weight). After 5 minutes, the ice bath was removed and the reaction was allowed to warm to ambient temperature. Once hydrogen gas evolution had ceased, as judged by an oil bubbler, the reaction mixture was cooled to 0° C., prior to the introduction of benzyl acetate (272 mg, 1.19 mmol). After 5 minutes, the ice bath was removed and the reaction was stirred for 15 hours. The bulk of the THF was removed under reduced pressure. The residue was then diluted with water and ether. The aqueous layer was extracted once with ether and the combined organics were washed with saturated brine. The organics were then dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of MeOH:DCM—0.5:99.5 to 5:95, to give the title compound. MS: m/z=378 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893079B2
Source datasetuspto-grants-2011_02
ORD IDord-cadee1e915964804bca8377abafc5a0d
Source noteuspto-grants-2011_02