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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726528Generated: October 30, 2026

Dichloromethane → 69853-71-0

https://huagongshe.com/reaction/726528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCholestan-3-ol, 5,6-epoxy-, (3b)-HCID 6453234—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
Product69853-71-0HCID 305339951.7%

Reaction Steps

Dichloromethane (50 ml) was added to pyridinium chlorochromate (2.78 g, 12.9 mmol) and molecular shieves (3 A) (4.37 g) and the mixture was stirred under a nitrogen atmosphere at room temperature for 15 minutes. To the resulting mixture was added a dichloromethane solution (30 ml) of 5,6-epoxycholesterol (α:β=5:1) (3.323 g, 8.6 mmol) prepared by the method of Fieser and Fieser (L. F. Fieser and H. Fieser, Reagents for Organic Synthesis, Vol. 1: 136, 1967) and the mixture was stirred for 3 hours. Ether (300 ml) was added to the reaction solution and the resulting solution was filtered through silica gel-magnesium sulfate. The organic layer was washed twice with 50 ml of a saturated saline solution and dried. The solvents were distilled off and the residue was purified by column chromatography. 6-Hydroxy-4-cholesten-3-one (α:β=5:1) was obtained as a colorless crystal from the hexane-ethyl acetate (5:1) eluate (yield: 51.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710143
Source datasetuspto-grants-1998_01
ORD IDord-8b16f032edba4b58a420620507372e2d
Source noteuspto-grants-1998_01