HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → [1-(Chlorocarbonyl)cyclobutyl]methyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Acetoxymethylcyclobutanecarboxylic Acid | HCID 15670507 | — |
| Product | [1-(Chlorocarbonyl)cyclobutyl]methyl acetate | HCID 15632048 | — |
Reaction Steps
Thionyl chloride (1.65 ml, 22.7 mmol) was added to neat 1-acetoxymethylcyclobutanecarboxylic acid (3.3 g, 18.9 mmol). The resulting mixture was stirred at room temperature for 1 hour, then heated on a steam bath for 5 minutes. After cooling, the excess thionyl chloride, HCl and SO2 were removed under reduced pressure (water aspirator). The remained residue was purified by distillation to provide the desired product as a colorless oil: bp 51°-3° C. (0.02 mm); NMR (CDCl3) δ=1.8~2.7 (9H, m containing a singlet at 2.04 δ), 4.40 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04847306 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-ec10160d12514ba6a0e8c785090ecde6 |
| Source note | uspto-grants-1989_07 |