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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAntimony pentachlorideHCID 24294—
ReactantSulfolaneHCID 31347—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantSodium BicarbonateHCID 516892—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902793
Source datasetuspto-grants-1990_02
ORD IDord-cf2f45f16e804537a733ac398c96c933
Source noteuspto-grants-1990_02