HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107530Generated: October 30, 2026
Chlorodifluoromethane → [4-(difluoromethoxy)phenyl](phenyl)methanone
https://huagongshe.com/reaction/2107530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [4-(difluoromethoxy)phenyl](phenyl)methanone | HCID 3315228 | — |
Reaction Steps
100 g of 4-hydroxybenzophenone and 200 g of sodium hydroxide are dissolved in a mixture of 1 l of water and 500 ml of dioxane. The mixture is heated to 70° C. and a vigorous stream of difluorochloromethane (Frigen 22) is introduced. After 2 hours, the mixture is cooled to room temperature and 1 l of water is added to the contents of the flask. The mixture is extracted three times using 1.2 l of chloroform each time, the chloroform phase is extracted by shaking with 1N sodium hydroxide solution, washed with water and the organic phase is dried using potassium carbonate. After stripping off the solvent and subsequent distillation under vacuum, 60 g (48%) of 4-difluoromethoxybenzophenone are obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935414 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-5586fcad8c2941bbb73dae7b93a7a6dc |
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| Source note | uspto-grants-1990_06 |
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