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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884220Generated: November 3, 2026

Chlorodifluoromethane → HCID 69898430, compound

https://huagongshe.com/reaction/1884220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodifluoromethaneHCID 6372—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 69898186HCID 69898186—
CatalystTetrabutylammonium BromideHCID 74236—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 69898430HCID 69898430—

Reaction Steps

Five hundred milligrams (500 mg) of N-[2-(3,4-dimethoxyphenyl)ethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide (1.46 mmol), 0.31 g (1.7 mmol) of 30% aqueous potassium hydroxide solution, 0.1 g (0.3 mmol) of tetrabutylammonium bromide and 10 ml of ethylene glycol dimethyl ether were mixed and chlorodifluoromethane gas was blown thereto at room temperature. After a small amount of 30% aqueous potassium hydroxide solution was further added, a sample was taken out from the reaction mixture and the disappearance of the starting material was confirmed by thin layer chromatograph analysis. Then, 5% hydrochrolic acid was added to the reaction mixture, which was followed by extracted with ethyl acetate, washed with 5% hydrochrolic acid, saturated aqueous sodium bicarbonate solution and saturated brine subsequently, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was washed with hexane to give 474 mg of N-[2-(3,4-dimethoxyphenyl) ethyl]-3-difluoromethoxy-2-(4-methylphenyl)acrylamide (the present compound 1005).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762321B2
Source datasetuspto-grants-2004_07
ORD IDord-b84830c6142c46ccb9f988b6667f8638
Source noteuspto-grants-2004_07