HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 67915270, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 53958006 | HCID 53958006 | — |
| Reactant | HCID 57132120 | HCID 57132120 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67915270 | HCID 67915270 | 63% |
Reaction Steps
A solution of (3S,4R)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-(3-triphenylphosphoranylidene-2-oxopropyl)-2-oxoazetidine (572 mg) and (2S)-1-allyloxycarbonyl-2-formylpyrrolidine (201.5 mg) in toluene (5 ml) was heated to reflex for three hours. Evaporation of the solvent gave a residue, which was taken up into ethyl acetate. The resultant precipitate was filtered off and washed with ethyl acetate. The filtrate and the washings were combined and evaporated in vacuo. The residue was chromatographed on silica gel (50 ml) eluting with a mixture of n-hexane and ethyl acetate (2:1-1:1-1:3 V/V) to give (3S,4R)-4-[(E)-4-{(2S)-1-allyloxycarbonylpyrrolidin-2-yl}-2-oxo-3-butenyl]-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-2-oxoazetidine (297.7 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081237 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-e9cc5985ae804c81a6f4ba6a483d3f3c |
| Source note | uspto-grants-1992_01 |