HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339507Generated: October 27, 2026
Hydrochloric Acid → 2-methoxy-5-(trifluoromethoxy)benzoic Acid
https://huagongshe.com/reaction/339507
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Methoxy-5-(trifluoromethoxy)benzaldehyde | HCID 2783364 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-methoxy-5-(trifluoromethoxy)benzoic Acid | HCID 2775286 | 91% |
Reaction Steps
To a stirred solution of 2-methoxy-5-trifluoromethoxybenzaldehyde (2.0 g, 9.09 mmol) and 50% KOH (4.1 ml) in MeOH (15 ml) at 65° C. was added dropwise hydrogen peroxide (30%, 7.4 ml) over 20 min. The reaction mixture was then stirred at 65° C. for 10 min., cooled to room temperature, acidified with 1 M HCl, and extracted with Et2O (3×40 ml). The combined organic extracts were washed with brine (35 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give a pale yellow viscous oil which solidified at room temperature overnight to give the title compound (1.95 g, 91%) as a pale yellow solid.
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-42d02c996db540dcaa03b8c4c3c23326 |
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| Source note | uspto-grants-2014_11 |
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