2-Bromobenzaldehyde → 1-(2-Bromophenyl)-2,2,2-trifluoroethan-1-ol
Reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].C[Si]([C:14]([F:17])([F:16])[F:15])(C)C.O.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]([OH:5])[C:14]([F:17])([F:16])[F:15]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 2-bromobenzaldehyde (27.0 g, 146.5 mmol) and trimethylsilyl-trifluoromethane (25.0 g, 175.8 mmol) in tetrahydrofuran (300 ml) was added drop-wise tetrabutylammonium fluoride (1 M in tetrahydrofuran, 5 ml, 5 mmol) at 0° C. After the addition, the mixture was stirred at room temperature for 2 hours. Further tetrabutylammonium fluoride hydrate (49.0 g, 175.8 mmol) was added and the mixture was stirred for 30 minutes. The solvent was evaporated in vacuo. The residue was dissolved in dichloromethane (200 ml) and washed with hydrochloric acid (2N aqueous solution) (4×100 ml). The organic layer was separated, washed with Na2CO3 (10% aqueous solution) (50 ml), dried over anhydrous MgSO4 (s), filtered and evaporated in vacuo to afford the crude title compound as a yellow oil (45.0 g, ˜100%).
Workup
- additionAfter the addition
- stirringthe mixture was stirred for 30 minutes
- customThe solvent was evaporated in vacuo
- dissolutionThe residue was dissolved in dichloromethane (200 ml)
- washwashed with hydrochloric acid (2N aqueous solution) (4×100 ml)
- customThe organic layer was separated
- washwashed with Na2CO3 (10% aqueous solution) (50 ml)
- dry with materialdried over anhydrous MgSO4 (s)
- filtrationfiltered
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-66468c3f96664c8d8f80ba5024ed57c6
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08134007B2
Reaction notes
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