HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657708Generated: October 29, 2026
Potassium Bromide → Benzhydryl 7-(2-thienylacetamido)-7-methoxy-3-acetoxymethyl-3-cephem-4-carboxylate
https://huagongshe.com/reaction/1657708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Benzhydryl 7-(2-thienylacetamido)-7-methoxy-3-methyl-3-cephem-4-carboxylate | HCID 131710295 | — |
| Catalyst | manganese(III) acetate dihydrate | HCID 160554 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzhydryl 7-(2-thienylacetamido)-7-methoxy-3-acetoxymethyl-3-cephem-4-carboxylate | HCID 54569218 | — |
Reaction Steps
Manganese (III) acetate (5.0 g.) in acetic acid (60 ml.) is heated to 70°C. under nitrogen. To the stirred solution is added benzhydryl 7-(2-thienylacetamido)-7-methoxy-3-methyl-3-cephem-4-carboxylate (4.0 g.) and potassium bromide (0.5 g.). The solution is maintained at 70°C. for about eight hours. The reaction mixture is cooled and manganese (II) acetate is filtered from the cooled solution. The solvent is removed under vacuum to afford benzhydryl 7-(2-thienylacetamido)-7 -methoxy-3-acetoxymethyl-3-cephem-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962231 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-24ca7da60ba6496f9f82d146ee291333 |
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| Source note | uspto-grants-1976_06 |
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