HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520264Generated: October 26, 2026
Ammonium Chloride → 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethan-1-ol
https://huagongshe.com/reaction/520264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,2,2-Trifluoro-4'-(trifluoromethyl)acetophenone | HCID 144683 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethan-1-ol | HCID 11390886 | 105.1% |
Reaction Steps
In a 50 mL two-neck flask, 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanone (2.0 g, 8.3 mmol) was dissolved in methanol (8 mL) and sodium borohydride (0.31 g, 8.3 mmol) was added carefully in portions with ice-bath cooling. The resultant colourless solution was stirred at RT for 2 hours and monitored by TLC. Upon the disappearance of all starting material, 5 mL of an aqueous saturated NH4Cl solution was slowly added to the reaction mixture with additional stirring for 10 min. The later was extracted 3 times with 20 mL of EtOAc and the organic fractions were combined and washed with 10 mL of brine, dried over Na2SO4, and filtered. The solvent was removed under reduced pressure to give 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (2.13 g, quantitative) as a colourless oil which was used with no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326513B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e683e4134cdc44cf945f314276bb5602 |
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| Source note | uspto-grants-2016_05 |
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