Dichloromethane → n1-[2-chloro-5-(trifluoromethyl)phenyl]-2,2-dichloroacetamide
Reaction equation
[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([C:9]([F:12])([F:11])[F:10])=[CH:5][C:3]=1[NH2:4].[CH2:13](N(CC)CC)[CH3:14].[Cl:20][CH:21]([Cl:25])[C:22](Cl)=[O:23].[CH2:26]([Cl:28])Cl>>[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([C:9]([F:10])([F:11])[F:12])=[CH:5][C:3]=1[N:4]1[CH2:14][CH:13]([CH2:26][Cl:28])[CH:21]([Cl:20])[C:22]1=[O:23].[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([C:9]([F:10])([F:11])[F:12])=[CH:5][C:3]=1[NH:4][C:22](=[O:23])[CH:21]([Cl:25])[Cl:20]Participants
Procedure
The intermediate N-[2'-chloro-5'-trifluoromethylphenyl]-3-chloro-4-chloromethyl-2-pyrrolidinone is prepared as follows: 50 g of 2-chloro-5-trifluoromethylaniline is combined with 34.8 g of triethylamine (TEA) and 200 ml of CH2Cl2. 48.6 g of dichloroacetyl chloride (DCAC) added dropwise while the mixture was kept at about 10° C. The mixture was stirred overnight forming a precipitate. The mixture was brought up to 1800 ml with CH2Cl2 and was washed 3 times (×) with 300 ml water, 3×300 ml 1.0N HCL and 3×300 ml saturated NaHCO3. The precipitate was dried over night with magnesium sulfate (MgSO4) and stripped, yielding 59 g of 2'-chloro-5'-trifluoromethyldichloroacetanilide. 58.3 g of the 2'-chloro-5'-trifluoromethyldichloroacetanilide and 37.2 g of potassium carbonate (K2CO3) were combined with 300 ml acetone and heated with stirring to reflux in a 2 liter flask equipped with a thermal reflux condenser, drop funnel and N2 bubbler. 39.1 g allyl bromide was added via the drop funnel at a constant temperature at 60° C. The mixture was refluxed for 2 hours and then stirred overnight. The mixture was filtered and stripped. 200 ml CH2Cl2 was added to the residue. This mixture was washed 3× with 100 ml H2O and 2× with 100 saturated NaCl solution. The filtrate was dried overnight in MgSO4 and stripped to yield 55 g of N-allyl-2'-chloro-5'-trifluoromethyldichloroacetanilide.
Workup
- customwas kept at about 10° C
- customforming a precipitate
- washwas washed 3 times (×) with 300 ml water, 3×300 ml 1.0N HCL and 3×300 ml saturated NaHCO3
- dry with materialThe precipitate was dried over night with magnesium sulfate (MgSO4)
Sources & evidence
- ORD record
- ord-18178f17e05e492daec3f97d855c6f6d
- Source dataset
- uspto-grants-1984_09
- Patent number
- US04469701
Reaction notes
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