HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226481Generated: October 30, 2026
Dimethylformamide → 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid
https://huagongshe.com/reaction/2226481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4,5-Trifluoro-3-hydroxybenzoic Acid | HCID 2734270 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid | HCID 15023781 | — |
Reaction Steps
20 ml of dimethylformamide, followed by 4.97 g (0.026 mole) of 2,4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F], were added in portions, whilst ice-cooling, to a solution of 2.18 g (0.052 mole) of sodium hydroxide in 5 ml of water. Thereafter the solution was stirred for 30 minutes, whilst ice-cooling. The reaction mixture was then transferred to a 200 ml stainless steel autoclave, and 100 ml of dimethylformamide containing 24.0 g (0.277 mole) of chlorodifluoromethane were added to it. The mixture was then stirred at between 100° and 110° C. for 5 hours under pressure. At the end of this time, the reaction mixture was poured into water and extracted with chloroform. The chloroform extracts were washed with water and dried over anhydrous sodium sulfate; the solvent was then removed by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of ethyl acetate and ethanol as the eluent, to afford 2.00 g of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05348961 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-accd265b35b24141903a1613dd04722e |
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| Source note | uspto-grants-1994_09 |
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