HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Trichloromethyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Trichloromethyl)benzoic acid | HCID 287015 | — |
| Product | 4-(Trichloromethyl)benzoyl chloride | HCID 84660 | — |
Reaction Steps
Reaction of 4-trichloromethylbenzoic acid with thionyl chloride affords 4-trichloromethylbenzoyl chloride, which, on reaction with diethylamine, affords 4-trichloro-methyl-N,N-diethylbenzamide. Following a procedure similar to that described in Preparation 5, reaction of the latter with s-butyl lithium and reaction of the resulting lithium salt with sulfur dioxide followed by sodium hydroxylamine-O-sulfonate affords 4-trichloromethyl-2-aminosulfonyl-N,N-diethylbenzamide, which, on heating in glacial acetic acid, affords 6-trichloromethylsaccharin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783589 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-95e1656ac2c54b87bb7bbd73a4b130e5 |
| Source note | uspto-grants-1998_07 |