HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440088Generated: October 26, 2026
Hydrochloric Acid → 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid
https://huagongshe.com/reaction/1440088
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid ethyl ester | HCID 15023780 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Difluoromethoxy)-2,4,5-trifluorobenzoic acid | HCID 15023781 | 102.7% |
Reaction Steps
20 ml of a 6% w/v aqueous solution of sodium hydroxide were added to a solution of 5.79 g (0.021 moles) of ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoate [(XXVI), X=X'=F, R16 =C2H5O] [prepared as described in step (b) above] in 40 ml of ethanol, and the mixture was left at room temperature overnight. The reaction mixture was then acidified by the addition of 3.5 ml of concentrated aqueous hydrochloric acid, and, after concentration by evaporation under reduced pressure, it was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure, to give 5.22 g of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid as a colorless powder, melting at 68°-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496951 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-7e0acb57e06145109a5a10b5ec3d595f |
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| Source note | uspto-grants-1996_03 |
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