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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111932Generated: November 2, 2026

Dimethylformamide → HCID 22765908, compound

https://huagongshe.com/reaction/1111932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhenyl chloroformateHCID 15891—
ReactantSodium BromideHCID 253881—
ReactantMethanol--water (1/1)HCID 22242641—
ProductHCID 22765908HCID 22765908—

Reaction Conditions

Temperature0 °C

Reaction Steps

Phenyl N,N-dimethylformamide bromide was prepared by dropwise addition of phenyl chloroformate (6.5 ml; 50 mmol) to a stirred solution of sodium bromide (5.14 g; 50 mmol) in dimethylformamide at 0°-5° C. Sodium chloride precipitated, and the resulting suspension was stirred at 0°-5° C. for 4 hours and then at room temperature overnight. The mixture was cooled to 0° C. and 16-deacetoxy-16β-(acetylthio)fusidic acid acetoxymethyl ester (6.07 g; 10 mmol) was added with stirring. After stirring at 0°-5° C. for 4 hours, the mixture was left at room temperature for a further 4 days. On dilution of the stirred reaction mixture with methanol-water 1:1 (75 ml) an oily product precipitated, which was washed repeatedly by decantation with methanol-water 1:1 and finally taken up in ether, dried, and evaporated in vacuo. The amorphous residue thus obtained was purified by dry column chromatography on silica gel (petroleum ether-ethyl acetate 85:15) to give the desired compound as a colourless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04119717
Source datasetuspto-grants-1978_10
ORD IDord-97e0a625f9c64beba09efdec33590f85
Source noteuspto-grants-1978_10