Chloroacetyl chloride → 2-chloro-N-(2,4-difluorophenyl)acetamide
Reaction equation
[F:1][C:2]1[CH:8]=[C:7]([F:9])[CH:6]=[CH:5][C:3]=1[NH2:4].C(N(CC)CC)C.[Cl:17][CH2:18][C:19](Cl)=[O:20]>C(Cl)Cl>[Cl:17][CH2:18][C:19]([NH:4][C:3]1[CH:5]=[CH:6][C:7]([F:9])=[CH:8][C:2]=1[F:1])=[O:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a cooled (0° C.) solution of 2,4-difluoroaniline, (1.5 g, 11.6 mmol) in DCM (50 mL) was added triethylamine (1.9 mL, 13.9 mmol) followed by 2-chloroacetyl chloride (1.0 mL, 12.8 mmol). The reaction was warmed to RT and stirred for 2 h. The reaction mixture was concentrated, redissolved in EtOAc (50 mL) and washed with brine (50 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to yield 2.2 g of crude product which was further purified by flash column chromatography using 1:1 EtOAc:hexanes as the eluent. 2.0 g of 2-chloro-N-(2,4-difluorophenyl)acetamide, (yield: 84%) was isolated.
Workup
- concentrationThe reaction mixture was concentrated
- dissolutionredissolved in EtOAc (50 mL)
- washwashed with brine (50 mL)
- dry with materialThe organic layer was dried over anhydrous Na2SO4
- concentrationconcentrated
- customto yield 2.2 g of crude product which
- customwas further purified by flash column chromatography
Sources & evidence
- ORD record
- ord-2c25e8cc92464de39c9046d7761104d9
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08133998B2
Reaction notes
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