Trifluoroacetic acid → 4-Bromo-2-fluoro-1-(1-methylethyl)benzene
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](O)([CH3:10])[CH3:9])=[C:4]([F:12])[CH:3]=1.C([SiH](CC)CC)C.FC(F)(F)C(O)=O>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:9])[CH3:10])=[C:4]([F:12])[CH:3]=1Participants
5
Procedure
To a solution of 2-(4-bromo-2-fluorophenyl)propan-2-ol (7.6 g, 32.8 mmol) dissolved in anhydrous CH2Cl2 (300 mL) at 25° C. was added triethylsilane (7.8 mL, 49.1 mmol), followed by trifluoroacetic acid (25 mL, 328 mmol). The resulting solution was stirred at that temperature for 45 min. The solvent was removed in vacuo and the residue was purified by flash column chromatography (0–10% EtOAc in hexanes) to give the desired product (5.7 g, 80% yield).
Workup
- customThe solvent was removed in vacuo
- customthe residue was purified by flash column chromatography (0–10% EtOAc in hexanes)
Sources & evidence
- ORD record
- ord-627df46d5ed24a25a8571d4bb2a69c72
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07148226B2
Reaction notes
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