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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425753Generated: October 28, 2026

Sodium hydride → HCID 59428169, compound

https://huagongshe.com/reaction/2425753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant4-{[tert-Butyl(diphenyl)silyl]oxy}cyclohexan-1-oneHCID 11416886—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 59428169HCID 59428169—

Reaction Steps

To a stirred suspension of sodium hydride (60% in mineral oil, 441 mg, 11.0 mmol) in dimethylsulfoxide (7 mL) was added trimethylsulfoxonium iodide (2.53 g, 11.5 mmol) at room temperature, and the mixture was stirred at room temperature for 30 min. To this mixture was added a solution of 4-{[tert-butyl(diphenyl)silyl]oxy}cyclohexanone (3.53 g, 10.0 mmol, Okamura, William H. et al., J. Org. Chem., 1993, 58, 600) in dimethylsulfoxide (35 mL) dropwise at room temperature, and the mixture was stirred at room temperature for 2 h. Then the mixture was diluted with water (600 mL), and extracted with diethyl ether (200 mL×4). The combined organic layer was dried over magnesium sulfate, and concentrated in vacuo. The residue was chromatographed on a column of silica gel eluting with ethyl acetate/n-hexane (1:10), and then purified with plate TLC eluting with ethyl acetate/n-hexane (1:15) to give 459 mg (13%, trans) and 390 mg (11%, cis) of the title compound as a colorless oil respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-75010ff6614f494a8d8a00f910298da5
Source noteuspto-grants-2011_06