HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199762Generated: November 2, 2026
Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| 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, 8 g of zinc bromide and 0.9 g of methanol. The mixture was heated at 60° C. for 80 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture were added 10 ml of water and 5 ml of methanol. Then, the mixture was adjusted to pH 7.5 with aqueous ammonia at a temperature of from 0° 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 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 0.71 g. The yield of the desired product was 29 %.
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-ac75637d49434fed9694c62a8231594c |
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| Source note | uspto-grants-1990_02 |
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