HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367818Generated: November 2, 2026
Hydrochloric Acid → 1-(2,4-Difluorophenyl)-2,2,2-trifluoroethan-1-ol
https://huagongshe.com/reaction/1367818
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Catalyst | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2,4-Difluorophenyl)-2,2,2-trifluoroethan-1-ol | HCID 61086802 | 117.9% |
Reaction Steps
2,4-Difluorobenzaldehyde (1.1 mL, 10.0 mmol) and (trifluoromethyl)trimethylsilane (1.77 mL, 12.0 mmol) were dissolved in THF (25 mL) and then cooled to 0° C. To this, 1M TBAF in THF (76 μL, 76 μmol) was added and the reaction mixture was allowed to warm to room temperature. After 3.25 h, 2.5M HCl (25 mL) was added. The reaction was stirred for 1 h and then extracted with ether. The organic layer was washed with brine and dried with Na2SO4. The solvent was removed under the reduced pressure to give 2,2,2-trifluoro-1-(2,4-difluoro-phenyl)ethanol (2.5 g) as a racemic mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893093B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-85b58a424fc4426299e11fe5d2c7df16 |
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| Source note | uspto-grants-2011_02 |
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