HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5,6-Dihydro-1,4-dithiin-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5,6-Dihydro-1,4-dithiin-2-carboxylic acid | HCID 20134009 | — |
| Product | 5,6-Dihydro-1,4-dithiin-2-carbonyl chloride | HCID 20134007 | — |
Reaction Steps
A suspension of 5,6-dihydro-1,4-dithiin-2-carboxylic acid (13.1 g) in thionyl chloride (60 cc) is gradually heated to reflux. After 30 minutes under reflux, the solution obtained is concentrated to dryness at 50° C. under reduced pressure (4 kPa) and the oily residue obtained is washed with cyclohexane (2×100 cc). The decanted oil is dried at 50° C. under reduced pressure (4 kPa). 5,6-Dihydro-1,4-dithiin-2-carbonyl chloride (15.8 g) is thereby obtained, and this is used as it is in the following operation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753941 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-b94411d15567428b9af5e861c86c60d4 |
| Source note | uspto-grants-1988_06 |