HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate → benzyl 4-[(2RS)-1-(tert-butyldimethylsilyl)-4-oxoazetidin-2-yl]but-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate | HCID 3862746 | — |
| Reactant | 1-(t-Butyldimethylsilyl)-4-(2-oxoethyl)-2-azetidinone | HCID 12804718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl 4-[(2RS)-1-(tert-butyldimethylsilyl)-4-oxoazetidin-2-yl]but-2-enoate | HCID 53904921 | 98.3% |
Reaction Steps
A mixture of (4RS)-1-(tert-butyl-dimethylsilyl)-4-(2-oxoethyl)-2-oxoazetidine (240 mg) and benzyl triphenylphosphoranylidene-acetate (521 mg) in dichloromethane (5 ml) was heated under refluxing for one hour. After removal of the solvent, the residue was chromatographed on silica gel (7 g) eluting with a mixture of dichloromethane and acetone (50:1) to give benzyl 4-[(2RS)-1-(tert-butyl-dimethylsilyl)-4-oxoazetidin-2-yl]but-2-enoate (373 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04383945 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-da2c8ee370184104b1b7d73df3a252fe |
| Source note | uspto-grants-1983_05 |