HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 20343950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 20343955 | HCID 20343955 | — |
| Product | HCID 20343950 | HCID 20343950 | — |
Reaction Steps
A suspension of 3.4 g of 1-acetyl-4-(2-phenylthiophenyl)piperidine-4-carboxylic acid, Example 15, in 5 ml of freshly distilled thionyl chloride is warmed on a steam bath for 5 minutes, effecting a clear solution. The excess thionyl chloride is removed at 50° C. under reduced pressure. The residue is recrystallized from a benzene-cyclohexane mixture to provide 1-acetyl-4-(2-phenylthiophenyl)piperidine-4-carbonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198419 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-5361e751ee4c401b92919af8a60cf14a |
| Source note | uspto-grants-1980_04 |