HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199759Generated: November 2, 2026
Carbon Tetrachloride → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Antimony pentachloride | HCID 24294 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| 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 carbon tetrachloride were added 2.72 g of 7-ACA, 15 g of antimony pentachloride and 1.40 g of methanol. The mixture was cooled at 10° 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 was added 150 ml of water. Then, the mixture was adjusted to pH 7.7 with sodium bicarbonate 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, and then concentrated by evaporation under reduced pressure so that a precipitate was formed. 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 0.61 g. The yield of the desired product was 25 %.
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-41af3223116f4b02a742de7839ad9b84 |
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| Source note | uspto-grants-1990_02 |
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