HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 70567532, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene ethyl acetate | HCID 21583983 | — |
| Reactant | HCID 70567759 | HCID 70567759 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70567532 | HCID 70567532 | 81% |
Reaction Steps
A mixture of (4 R,S)-4-vinylthio-(1-hydroxyethyl-2-ethoxycarbonyl)-2-oxo-azetidine (1.01 g, 4.13 mmole), acetic anhydride (1 ml, 10.6 mmole), and Et3N (0.7 ml, 5 mmole) dissolved in methylene chloride (60 ml) was allowed to stand overnight at room temperature. The reaction mixture was then washed with brine (3 times), and dried on Na2SO4. Evaporation of the solvent left a residue which, after column chromatography (SiO2, 10% ethyl acetate-benzene), yielded 950 mg (3.31 mmole, 81%) of an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04269771 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-dd2cd102ade94376aa285f5a23a92c7b |
| Source note | uspto-grants-1981_05 |