HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704259Generated: October 29, 2026
Formic Acid → Benzhydryl 7-formamido-3-hydroxycepham-4-carboxylate
https://huagongshe.com/reaction/704259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzhydryl 7-amino-3-hydroxycepham-4-carboxylate | HCID 67948072 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzhydryl 7-formamido-3-hydroxycepham-4-carboxylate | HCID 86743417 | — |
Reaction Steps
Formic acid (0.4 ml) and acetic anhydride (1 ml) were stirred at 40° C. for 30 minutes. The reaction mixture was cooled in an ice-water bath and added dropwise to a mixture of benzhydryl 7-amino-3-hydroxycepham-4-carboxylate (1.0 g) in methylene chloride (30 ml) at 3° C. The mixture was stirred at 3° C. for 10 minutes and adjusted to pH 7.0 with 5% aqueous solution of sodium bicarbonate, washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give benzhydryl 7-formamido-3-hydroxycepham-4-carboxylate (1.05 g) as powder.
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-624f8c5376b544588acf02caa1b7a678 |
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| Source note | uspto-grants-1991_01 |
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