HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(Trichloromethyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 52382-30-6 | HCID 21964677 | — |
| Product | 2-(Trichloromethyl)benzoyl chloride | HCID 3016752 | — |
Reaction Steps
Similarly, reaction of 2-trichloromethylbenzoic-acid with thionyl chloride affords 2-trichloromethylbenzoyl-chloride, which, on reaction with diethylamine, affords 2-trichloromethyl-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 hydroxyl-amine-O-sulfonate affords 2-trichloromethyl-6-aminosulfonyl-N,N-diethylbenzamide, which, on heating in glacial acetic acid, affords 4-trichloromethylsaccharin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563163 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-531a8abeb15e4c8a9ef0b97c2eb70fa5 |
| Source note | uspto-grants-1996_10 |