HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073367Generated: November 1, 2026
Benzaldehyde → (S)-alpha-(Trifluoromethyl)benzyl alcohol
https://huagongshe.com/reaction/1073367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (S)-alpha-(Trifluoromethyl)benzyl alcohol | HCID 95556 | 88% |
Reaction Steps
Benzaldehyde was reacted with trifluoromethyltrimethylsilane as in Example 10. After a reaction time of 5 hours, 20 ml of water were added, and the reaction mixture was heated briefly to 80° C. 50 ml of hexane were then added. The reaction mixture was then extracted twice with 100 ml of water, and the resultant organic phase was dried over Na2SO4. On distillation of the crude product, 15.4 g (88% yield) of 1-phenyl-2,2,2-trifluoroethanol (boiling point 68°-69° C./6 mbar) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968848 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-15bdb696565d45b18391453cc4922b27 |
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| Source note | uspto-grants-1990_11 |
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