Hydrochloric Acid → HCID 22760593, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[S:11](=[O:18])(=[O:17])[N:12]([CH2:15][CH3:16])[CH2:13][CH3:14].[ClH:19]>S(Cl)(Cl)=O>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([Cl:19])=[O:7])=[CH:4][C:3]=1[S:11](=[O:18])(=[O:17])[N:12]([CH2:15][CH3:16])[CH2:13][CH3:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
39 g of 4-chloro-3-diethylsulfamoylbenzoic acid were boiled under reflux in 200 ml of thionyl chloride until the development of HCl had finished and the thionyl chloride was then distilled off under reduced pressure. 4-chloro-3-diethylsulfamoylbenzoyl chloride was obtained as fair yellow oil.
Workup
- distillationthe thionyl chloride was then distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-7f0ddc3cf5a240fdb0df262abeda11c1
- Source dataset
- uspto-grants-1978_11
- Patent number
- US04125614
Reaction notes
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