HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 2-(5-Chloropentyl)-5-acetylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-(5-Acetyl-2-furanyl)pentanol | HCID 10330303 | — |
| Product | 2-(5-Chloropentyl)-5-acetylfuran | HCID 10353215 | 60% |
Reaction Steps
5-(5-Acetyl-2-furanyl)pentanol (9.8 g), 13.1 g of triphenylphosphine and 100 ml of carbon tetrachloride were combined and heated at reflux for 4 hours. The reaction mixture was concentrated in vacuo, and the residue was dissolved in ether and filtered. The filtrate was concentrated and the residue distilled twice to give 2-(5-chloropentyl)-5-acetylfuran, b.p. 100°-102° C. (0.05 mm) in 60% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04861791 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-76cedab43c394c8180bbc60409b1dfe0 |
| Source note | uspto-grants-1989_08 |