HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884220Generated: November 3, 2026
Chlorodifluoromethane → HCID 69898430, compound
https://huagongshe.com/reaction/1884220
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 69898186 | HCID 69898186 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 69898430 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762321B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-b84830c6142c46ccb9f988b6667f8638 |
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| Source note | uspto-grants-2004_07 |
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