HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-Cyclohexylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Cyclohexylbenzoic acid | HCID 88337 | — |
| Product | 4-Cyclohexylbenzoyl chloride | HCID 21890847 | — |
Reaction Steps
Reaction of 4-cyclohexylbenzoic acid with thionylchloride affords 4-cyclohexylbenzoyl chloride, which, on reaction with diethylamine, affords 4-cyclohexyl-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-cyclohexyl-2-aminosulfonyl-N,N-diethylbenzamide, which, on heating in glacial acetic acid, affords 6-cyclohexyl saccharin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563163 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-6929a0432e7d4ad891d4777c6def76d3 |
| Source note | uspto-grants-1996_10 |