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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367456Generated: November 2, 2026

Thiophenol → HCID 66918859, compound

https://huagongshe.com/reaction/1367456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86649015HCID 86649015—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66918859HCID 66918859—

Reaction Steps

To a solution of the thiophenol (0.41 mmol) in THF (4 ml) was added NaH (55% in oil, 0.41 mmol) at 22° C. and stirring was continued until gas evolution ceased. To the mixture was added a solution of (1R,2R,4R)-4-methanesulfonyloxy-2-(morpholine-4-carbonyl)-cyclopentanecarboxylic acid ethyl ester (0.28 mmol) in THF (4 ml) and stirring was continued at 50° C. until completion of the reaction. The mixture was partitioned between ethyl acetate and water, the organic layer was dried, evaporated and the residue chromatographed on silica using mixtures of cyclohexane and ethyl acetate to give the title compound as pale yellow oil. MS: 364.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-adbe35b754aa4efb9c3b3f935d0ff495
Source noteuspto-grants-2011_02