Phosphorus pentachloride → HCID 15121251, compound
Reaction equation
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[NH:9][C:10](=O)[CH2:11][CH3:12].P(Cl)(Cl)(Cl)(Cl)[Cl:17]>C1(C)C=CC=CC=1>[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]=[C:10]([Cl:17])[CH2:11][CH3:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 18 g of the product of Step A in 150 ml of toluene was added over 15 minutes to a suspension of 19 g of phosphorus pentachloride in 23 ml of toluene and after gas evolution ceased, the mixture was refluxed for 11/2 hours. The toluene was evaporated under reduced pressure to obtain 19 g of N-(2-trifluoromethylphenyl)-propanimidoyl chloride in the form of a yellow oil which was used as is for the next step.
Workup
- temperaturethe mixture was refluxed for 11/2 hours
- customThe toluene was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-1d45f5beb88c4c55be33d4f5093c0c2b
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04107310
Reaction notes
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