HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-Pentylcyclobutanecarboxylic acid chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cyclobutanecarboxylic acid, 3-pentyl- | HCID 47799 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Pentylcyclobutanecarboxylic acid chloride | HCID 15340221 | 91.1% |
Reaction Steps
A reaction vessel was charged with 140 g of thionyl chloride and 100 ml of benzene, and 100 g of 3-pentylcyclobutanecarboxylic acid was added dropwise under reflux with stirring. The resultant mixture was refluxed with stirring for 8 hours and the excess thionyl chloride was azeotropically distilled off with benzene and the residue was distilled under reduced pressure to obtain 101 g (yield 91%) of 3-pentylcyclobutanecarboxylic acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545747 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-71457bf1bded4e23b0cfd3ec1725f6c1 |
| Source note | uspto-grants-1996_08 |