HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 18781991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 4-Acetoxy-2-azetidinone | HCID 119981 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 18781954 | HCID 18781954 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18781991 | HCID 18781991 | 48% |
Reaction Steps
Sodium (1.15 g) was added to allyl alcohol (50 ml) and this solution treated with allyl 4-(acetylthio)butanoate (10.Og) at room temperature for 20 mins. 4-Acetoxyazetidinone (6.5 g) was added and stirring continued at 20° C. for 1 h The resulting mixture was poured into excess ethyl acetate and the layers separated. The organic layer was washed with water, brine, dried (MgSO4), filtered and evaporated. The residue was chromatographed on silica gel (diethyl ether) to give the title compound as a yellow oil, 5.5 g. 48% yield
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06071899 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-92e768b62bcd474d93a2b9fc36d38b37 |
| Source note | uspto-grants-2000_06 |