Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 56614980 | HCID 56614980 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86741780 | HCID 86741780 | — |
Reaction Steps
A solution of 687 mg (1.29 mmole) of 2-[(3S,4R)-4-(benzthiazol-2-yldithio)-3-phenoxyacetoxy-2-oxoazetidin-1-yl]-3-methylcrotonic acid methyl ester in 14 ml of dimethylformamide is added to a solution, cooled to -20°, of 76 mg (2 mmole) of sodium borohydride in 10 ml of dimethylformamide and the mixture is stirred at the same temperature for 10 minutes. 7 ml of freshly distilled acetyl bromide are added to the reaction mixture, which is further stirred at 0° for 40 minutes. After adding 400 ml of benzene, the reaction mixture is washed in succession with aqueous sodium bicarbonate solution, water and sodium chloride solution, dried over sodium sulphate and concentrated by evaporation in vacuo. After chromatography over silica gel with toluene/ethyl acetate (19:1) the residue yields the title compound in the form of an oil, which is further purified on silica gel plates with toluene/ethyl acetate (4:1). The title compound is obtained in oily form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04692442 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-f87edf64806b48a3833bfd648421e3cd |
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| Source note | uspto-grants-1987_09 |
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