HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904980Generated: November 3, 2026
Potassium Hydroxide → 2-(4Ethoxyphenyl)-3,3,3-trifluoropropanal
https://huagongshe.com/reaction/1904980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 3-(4-ethoxyphenyl)-2,3-epoxy-4,4,4-trifluorobutyrate | HCID 14580830 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4Ethoxyphenyl)-3,3,3-trifluoropropanal | HCID 10799561 | 62% |
Reaction Steps
Into a solution of 11.41 g of potassium hydroxide in 80 ml of ethanol and 20 ml of water, 29.55 g of methyl 3-(4-ethoxyphenyl)-2,3-epoxy-4,4,4-trifluorobutyrate was added with ice-cooling. The reaction solution was stirred at room temperature for 17 hours. Thereafter, the reaction solution was poured into ice water. The resulting solution was washed with diethyl ether and adjusted to pH 3 with 10% HCl and extracted twice with diethyl ether. The ether layers were combined and washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure and the residue was subjected to distillation under a reduced pressure by heating in an oil bath (130°-140° C.) to obtain 14.66 g of the desired aldehyde (b.p. 100°-105° C./0.3 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04840971 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-5545ce6b9df248cc915994ddfcd0113c |
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| Source note | uspto-grants-1989_06 |
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