HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl 3-furyl(hydroxy)acetate → Butyl 2-(fur-3-yl)-2-oxo-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl 3-furyl(hydroxy)acetate | HCID 12335665 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Butyl 2-(fur-3-yl)-2-oxo-acetate | HCID 13986137 | 83.4% |
Reaction Steps
A mixture of 39.6 g of butyl fur-3-yl-glycolate and 8.6 g of lead tetraacetate in 400 ml of absolute benzene is refluxed for 8 hours. After cooling to room temperature, the salts are filtered off and washed with benzene, and the combined benzene phases are shaken with a 10% strength sodium bicarbonate solution and a saturated sodium chloride solution. After drying over sodium sulphate, filtering off and concentrating, the oily residue is distilled in vacuo. 32.7 g (83%) of an oil, boiling point 80° C. (0.3 Torr), nD20 =1.477, are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04757085 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-56a45a5dfd974825b9f1604ecb08b06a |
| Source note | uspto-grants-1988_07 |