HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199764Generated: October 30, 2026
Hydrochloric Acid → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Antimony pentachloride | HCID 24294 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| 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 13 ml of sulfolane were added 2.72 g of 7-ACA, 3.5 g of methanol, 8.0 g of zinc chloride and 2.9 g of antimony pentachloride. The mixture was heated at 50° C. for 80 min while stirring 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 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 concentrated by evaporation under reduced pressure, and adjusted to pH 7 with 1N HCl. Then, the mixture was applied to a column packed with XAD-II (packing material for reversed phase adsorption chromatography manufactured and sold by Rohm and Haas Co., U.S.A.). Then, 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 1.73 g. The yield of the desired product was 71 %.
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-cf2f45f16e804537a733ac398c96c933 |
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| Source note | uspto-grants-1990_02 |
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