Phosphorus pentachloride → HCID 54261612, compound
Reaction equation
[C:1]1([S:7]([N:10]([CH3:22])[NH:11][C:12](=O)[C:13]2[C:18]([Cl:19])=[CH:17][CH:16]=[CH:15][C:14]=2[Cl:20])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:24]>ClCCCl>[C:1]1([S:7]([N:10]([CH3:22])[N:11]=[C:12]([Cl:24])[C:13]2[C:18]([Cl:19])=[CH:17][CH:16]=[CH:15][C:14]=2[Cl:20])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Into a 1 L three necked round bottom flask equipped with a magnetic stirrer and condenser under an atmosphere of nitrogen was added N-benzenesulfonyl-N-methyl-2,6-dichlorobenzoyl hydrazine (35.9 g, 0.10 mol), 1,2-dichloroethane (500 mL), and phosphorus pentachloride (31.2 g, 0.15 mol). The temperature of the mixture was raised to the point of reflux and was allowed to stir for 30 min. The solvent was removed in vacuo and the residue dissolved in methylene chloride and carefully diluted with water. The organic phase was washed with water, brine, dried (Na2SO4) and the solvent removed in vacuo to give an oil which solidified when triturated with ethyl acetate/hexanes mixture to give 36.1 g (95.7% yield) N-benzenesulfonyl-N-methyl-2,6-dichlorobenzhydrazonoyl chloride as a white crystalline solid: mp 103-104° C.; 1H NMR (CDCl3) δ 7.9 (m, 2H), 7.4-7.7 (m, 3H), 7.2-7.4 (m, 3H), 3.1 (s, 3H).
Workup
- temperatureThe temperature of the mixture was raised to the point
- temperatureof reflux
- customThe solvent was removed in vacuo
- dissolutionthe residue dissolved in methylene chloride
- additioncarefully diluted with water
- washThe organic phase was washed with water, brine
- dry with materialdried (Na2SO4)
- customthe solvent removed in vacuo
- customto give an oil which
- customtriturated with ethyl acetate/hexanes mixture
Sources & evidence
- ORD record
- ord-5817d65ee60b49b897eecccea25c513e
- Source dataset
- uspto-grants-2000_01
- Patent number
- US06015826
Reaction notes
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