HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199766Generated: November 1, 2026
Sodium Sulfide → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199766
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Bismuth trichloride | HCID 24591 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| 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, 2.2 g of methanol, 9.0 g of bismuth trichloride and 5.9 g of ferric chloride. The mixture was heated at 30° C. for 160 min to advance a reaction After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture was added 50 ml of water. Then, the mixture was adjusted to pH 1 with sodium bicarbonate and, then, further adjusted to pH 7.5 with sodium sulfide while cooling on ice. 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 the mixture was added 50 ml of methanol, and the mixture was allowed to stand at 5° C. for 10 hours, thereby to 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 1.37 g. The yield of the desired product was 56 %.
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-b5e58011fe33457b8b907c110b197fe1 |
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| Source note | uspto-grants-1990_02 |
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