HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199765Generated: October 30, 2026
Hydrochloric Acid → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid | HCID 12833023 | — |
Reaction Steps
To 10 ml of nitromethane were added 2.72 g of 7-ACA, 2.7 g of methanol, 5.0 g of zinc chloride and 4.0 g of ferric chloride. The mixture was heated at 50° C. for 30 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture was added 150 ml of water. Then, the mixture was adjusted to pH 7.5 with sodium bicarbonate at a temperature of from 2° C. to 5° C. The resulting precipitate was filtered off, and then washed with water. The filtrate was combined with the washings. The resulting mixture was concentrated by evaporation under reduced pressure, and adjusted to pH 7 with 1N HCl. Then, the mixture was applied to the same column as used in Example 2. The elution was conducted using water as an eluent to obtain an eluate. The eluate was adjusted to pH 3.5 with 36 % hydrochloric acid to thereby form a precipitate. The precipitate was collected by filtration, and washed with 10 ml of cold water and, then, with 10 ml of cold methanol to obtain the desired product, namely 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. The amount of the desired product was 1.63 g. The yield of the desired product was 67 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04902793 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-ab1ebc86ca00464c93f139650ab7bc33 |
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| Source note | uspto-grants-1990_02 |
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