HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-[(Phenylmethyl)thio]benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Benzylsulfanyl)benzoic acid | HCID 264182 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[(Phenylmethyl)thio]benzoyl chloride | HCID 20067340 | 94.1% |
Reaction Steps
A suspension of 100 g of 2-[(phenylmethyl)thio]benzoic acid and 97.6 g of thionyl chloride in 800 ml of benzene was refluxed for about three hours then evaporated to dryness under vacuum. The residue was triturated with hexane to yield 101.2 g of 2-[(phenylmethyl)thio]benzoyl chloride, m.p. 113° to 116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04995901 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-f6ab892768b743d48204bed41050d080 |
| Source note | uspto-grants-1991_02 |