HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Benzhydrylthioacetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178526172 | HCID 178526172 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzhydrylthioacetyl chloride | HCID 18769441 | — |
Reaction Steps
19.5 g (0.076 mol) of benzhydrylthioacetic acid in 114 ml of benzene are placed in a three-necked flask provided with a condenser and a dropping funnel. The mixture is heated and 19 ml of thionyl chloride are added drop by drop. Once the addition is complete, the reflux is continued for about 1 hour, cooling and filtering are carried out and the benzene and the excess thionyl chloride and then evaporated. In this way, a clear orange oil is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04177290 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-2abe3ad6ca93492494aa196319ebb94c |
| Source note | uspto-grants-1979_12 |