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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantAntimony pentachlorideHCID 24294—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023—

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902793
Source datasetuspto-grants-1990_02
ORD IDord-41af3223116f4b02a742de7839ad9b84
Source noteuspto-grants-1990_02