HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399836Generated: November 3, 2026
Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/2399836
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Monomethyl sulfate | HCID 6412 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid | HCID 12833023 | 113.9% |
Reaction Steps
22.0 g of a methanolic solution of methoxysulfonic acid (prepared as described in Preparation 3) and 2.10 g of trimethyl borate were added to 30 ml of dimethyl carbonate. The mixture was cooled to 10° C. Next, 2.74 g of 7-ACA were added and the mixture was stirred at 10° C. for 1.5 hours. After completion of the reaction, the reaction mixture was poured over crushed ice, and aqueous ammonia was added thereto to adjust the pH to 3.5. The crystals precipitated were filtered off, washed with water and dried to afford 2.80 g of crude 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. Water was added to the crude crystals, and then aqueous ammonia was added to adjust the pH to 8. The mixture was then decolored using activated carbon. The activated carbon was filtered off and the filtrate was adjusted to pH 3.5 with hydrochloric acid. The crystals precipitated were filtered off, washed with water and dried to give 2.11 g (yield 86%) of the desired compound in a highly pure form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451675 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-3bc791c7f3324774b6788bdafb83a70b |
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| Source note | uspto-grants-1995_09 |
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