HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499126Generated: November 2, 2026
Hydrochloric Acid → 1-(5-Bromo-[1,1'-biphenyl]-2-yl)-2,2,2-trifluoroethanol
https://huagongshe.com/reaction/1499126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 5-Bromo-[1,1'-biphenyl]-2-carbaldehyde | HCID 54197319 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Bromo-[1,1'-biphenyl]-2-yl)-2,2,2-trifluoroethanol | HCID 117942108 | — |
Reaction Steps
To a solution of 5-bromo-[1,1′-biphenyl]-2-carbaldehyde (1.9 g, 7.3 mmol) and was added TMSCF3 (1.2 g, 8.7 mmol) in THF (20 mL) and cooled to 0° C. To this solution was added TBAF (1.46 mL, 1M in THF) and the reaction mixture was warmed to RT for 3 h. After this time, the mixture was treated with 3 N HCl (5 mL) and stirred for 12 h. Then the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered, concentrated in vacuo and purified by normal phase silica gel column (EtOAc:PE=1:10) to afford 1-(5-bromo-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199994B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-8f7da66d5a9548858237e03e2a8ca154 |
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| Source note | uspto-grants-2015_12 |
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