HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441353Generated: October 30, 2026
1-Phenyl-1-propanone → alpha-Ethyl-alpha-phenyl-3-(trifluoromethyl)benzenemethanol
https://huagongshe.com/reaction/441353
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenyl-1-propanone | HCID 7148 | — |
| Reactant | Benzene, 1-bromo-3-(trifluoromethyl)- | HCID 9817 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Ethyl-alpha-phenyl-3-(trifluoromethyl)benzenemethanol | HCID 41870 | — |
Reaction Steps
A solution of 37.5 g. of propiophenone in 200 ml. of dry ether is added dropwise to a -10° C. Grignard solution prepared from 13.6 g. of magnesium turnings and 126 g. of 3-trifluoromethyl-bromobenzene in 182 ml. of dry ether. The reaction mixture is stirred at 0° C. for 30 minutes, thereafter refluxed for 1 hour. The mixture is cooled to 0° C., and the Grignard complex is decomposed with a 10% aqueous ammonium chloride solution. The etheral phase is separated, washed until neutral, and dried over anhydrous sodium sulfate. The solvent is evaporated, and the residual oil is subjected to fractional distillation in vacuo. This way 57.3 g. of 3-trifluoromethyl-α-ethyl-benzhydrol are obtained; b.p.: 106°-108° C./0.03 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04039589 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-66c50e8ed13843339ccd23e268e58754 |
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| Source note | uspto-grants-1977_08 |
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