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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119941Generated: October 31, 2026

HCID 11241422, compound → HCID 12447362, compound

https://huagongshe.com/reaction/2119941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11241422HCID 11241422—
SolventDichloromethaneHCID 6344—
ProductHCID 12447362HCID 1244736273.6%

Reaction Steps

To a solution of (1R,2R)-2-benzoyloxy-1,2-epoxycyclohexane (0.030 g, 0.137 mmol, 93% ee) in anhydrous CH2Cl2 (0.4 mL) was added YbCl3 (0.0038 g, 0.0137 mmol). Upon stirring at room temperature for 30 min, the reaction mixture was quenched with saturated NaHCO3 solution, extracted with ether, dried over anhydrous Na2SO4, filtered, concentrated, and purified on buffered silica gel (0.5-1% Et3N) by flash column chromatography [EtOAc-CH2Cl2-hexane (3:7:40)] to afford (S)-2-benzoyloxy cyclohexanone (0.022 g, 73% yield, 88% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686483B2
Source datasetuspto-grants-2004_02
ORD IDord-f3a1dd6c94ff428bb5872a4455482e4e
Source noteuspto-grants-2004_02