HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339511Generated: October 30, 2026
Hydrochloric Acid → 4-(3,3,3-Trifluoropropoxy)benzoic acid
https://huagongshe.com/reaction/339511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(3,3,3-Trifluoropropoxy)benzaldehyde | HCID 58342188 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(3,3,3-Trifluoropropoxy)benzoic acid | HCID 58111655 | 83% |
Reaction Steps
To a stirred solution of 50% w/v KOH (0.8 ml) and 4-(3,3,3-trifluoropropoxy)benzaldehyde (0.4 g, 1.83 mmol) in MeOH (4 ml) at 65° C. was added dropwise over 20 min aqueous hydrogen peroxide (30 wt. % in water, 1.5 ml). On completion of the addition the reaction mixture was heated at 65° C. for a further 10 min. On cooling to room temperature, the reaction mixture was acidified with 1 M HCl and extracted with Et2O (3×25 ml). The combined organic extracts were washed with brine (25 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give the title compound (0.36 g, 83%) as a colourless solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895313B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3ddbd9232e7c4b4c9a40e16e6fa7bf6c |
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| Source note | uspto-grants-2014_11 |
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