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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199081Generated: October 30, 2026

Dichloromethane → HCID 88684209, compound

https://huagongshe.com/reaction/2199081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron trifluoride etherateHCID 8000—
Reactant4-MethoxybenzenethiolHCID 12765—
ReactantHCID 13421116HCID 13421116—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 88684209HCID 88684209—

Reaction Steps

To a solution of 9-fluoro-11β-hydroxyandrosta-1,4-diene-3,17-dione (3.18 g) in a mixture of dry dichloromethane (40 ml) and glacial acetic acid (40 ml) containing p-methoxybenzenethiol (5.6 g) is added boron trifluoride etherate (3.0 ml) and the resulting solution is stirred for 1.5 hours. It is then poured into water (500 ml) and extracted with chloroform. The chloroform extracts are combined, washed with saturated sodium bicarbonate solution and water, dried (MgSO4) and concentrated in vacuo to a syrupy residue. This is absorbed on a column of silica gel (50 g) made up in chloroform-hexane (1:1) and the column is eluted successively with chloroform-hexane (1:1), chloroform and chloroform-ethyl acetate mixtures (95:5 and 90:10) to elute successively p-methoxybenzenethiol contaminated with some steroidal impurities, the title compound (3.0 g), a small amount of an undentified compound and unreacted starting material (1.0 g). The 3.0 g of material is refluxed with ethyl acetate (30 ml), cooled and filtered to leave the analytical specimen (dried at 0.3 mm of Hg, 100° C., 18 hours) of the title compound (2.8 g), melting point 209°-211° C., with consistent spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04361559
Source datasetuspto-grants-1982_11
ORD IDord-2f1d7825931d42bb8adad7bd0633718c
Source noteuspto-grants-1982_11