Dimethyl Sulfoxide → 2-Bromo-4-fluorobenzaldehyde
Reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Br:11][C:12]1[CH:17]=[C:16]([F:18])[CH:15]=[CH:14][C:13]=1[CH2:19][OH:20].C(N(CC)CC)C>ClCCl>[Br:11][C:12]1[CH:17]=[C:16]([F:18])[CH:15]=[CH:14][C:13]=1[CH:19]=[O:20]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
To a −78° C. cooled solution of oxalyl chloride (8.43 ml; 96.58 mmol) in anhydrous dichloromethane (300 ml) was added dropwise dimethyl sulfoxide (13.71 ml; 193.16 mmol). The mixture was stirred at −78° C. for 5 minutes then a solution of (2-bromo-4-fluorophenyl)methanol (Description 77, 18 g; 87.8 mmol) in anhydrous dichloromethane (150 ml) was added slowly. The resulting mixture was stirred at −78° C. for 15 minutes then triethylamine (36.71 ml; 263.4 mmol) was added and the mixture allowed to warm to room temperature over 1 hour. The mixture was washed with water (2×500 ml), saturated NaCl (200 ml), dried over Na2SO4, filtered through a 2 inch plug of silica gel and evaporated to give the title compound (16 g, 89%) as a white solid.
Workup
- stirringThe resulting mixture was stirred at −78° C. for 15 minutes
- temperatureto warm to room temperature over 1 hour
- washThe mixture was washed with water (2×500 ml), saturated NaCl (200 ml)
- dry with materialdried over Na2SO4
- filtrationfiltered through a 2 inch plug of silica gel
- customevaporated
Sources & evidence
- ORD record
- ord-b50cc4ec8b3c4018ba3284b118ce519c
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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