HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339515Generated: October 25, 2026
Hydrochloric Acid → 4-(2-Fluoroethoxy)benzoic acid
https://huagongshe.com/reaction/339515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(2-Fluoroethoxy)benzaldehyde | HCID 15058649 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Fluoroethoxy)benzoic acid | HCID 51357093 | 63% |
Reaction Steps
To a stirred solution of 50% w/v KOH (1.3 ml) and 4-(2-fluoroethoxy)benzaldehyde (0.5 g, 2.98 mmol) in MeOH (6 ml) at 65° C. was added dropwise over 20 min aqueous hydrogen peroxide (30 wt. % in water, 2.45 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 (3×30 ml). The combined organic extracts were washed with brine (30 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give a solid which was purified by flash chromatography (1:1 Hexane/EtOAc) to give the title compound (0.278 g, 63%) as a colourless 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-db5125dd0639494b9ee21fc6a3c480e7 |
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| Source note | uspto-grants-2014_11 |
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