HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167980Generated: November 3, 2026
Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1167980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid | HCID 12833023 | 26% |
Reaction Steps
10 g of 7-aminocephalosporanic acid was added to 80 ml of methylene chloride and the resulting mixture was cooled to 0° C., and then, 36.2 m of methanesulfonic acid was added slowly thereto. 7.4 ml of trimethyl borate was added thereto at the above temperature and the resulting mixture was stirred at 0 ° C. for 5 hours, and then, the resulting mixture was added to ice-water. The pH of the mixture was adjusted to 3.5 with aqueous ammonia. The ocherous solid formed was isolated by filtration and washed with water. The wet solid was dispersed in water and adjusted the pH to 8 with aqueous ammonia to dissolve the solid in water. Thereafter, the pH of the resulting mixture was adjusted to 3.5 with 3N hydrochloric acid. The resulting mixture was filtered to obtain crystals and the crystals were washed with water and then, dried overnight in a vacuum to give 2.32 g of 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid as an ocherous solid (Yield: 26% and Purity: 95.5%). H-NMR data was equal to that of the compound prepared in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620930B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-c8abbdbea689452cb0bcebf53af22b5d |
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| Source note | uspto-grants-2003_09 |
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