HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704261Generated: October 29, 2026
Potassium Carbonate → Benzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylate
https://huagongshe.com/reaction/704261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate | HCID 88528581 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylate | HCID 88528775 | — |
Reaction Steps
Mesyl chloride (0.66 ml) and potassium carbonate (1.38 g) were added to a solution of benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate (2.05 g) in N,N-dimethylformamide (6 ml) at -30° C. The mixture was stirred at -30° C. for 30 minutes. Mesyl chloride (0.4 ml) was added to the mixture. The reaction mixture was stirred at -30° C. for 20 minutes, poured into ice-water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and filtered, and the filtrate was evaporated in vacuo. The residue was dissolved in a small amount of ethyl acetate and the mixture was subjected to column chromatography on silica gel and eluted with a mixture of benzene and ethyl acetate (1:1). The eluent was evaporated in vacuo. The residue was triturated with diisopropyl ether to give benzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylate (0.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985555 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-0da1846da2e04d90ae4f05bb7803ae7f |
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| Source note | uspto-grants-1991_01 |
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