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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087248Generated: October 31, 2026

Sulfuric Acid → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1087248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTrimethyl borateHCID 8470—
ReactantSodium ThiosulfateHCID 24477—
ReactantSulfolaneHCID 31347—
Reactant7-Aminocephalosporanic acidHCID 441328—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023—

Reaction Conditions

Temperature30 °C

Reaction Steps

To 20 ml of sulfolane were added 1.41 g of 7-ACA, 1.96 g of ferric chloride, 0.29 ml of concentrated sulfuric acid and 1.22 ml of trimethyl borate. The mixture was heated at 30° C. for 3 hours to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 0° C. To the reaction mixture were added 30 ml of water, 10 ml of methanol and 3.04 g of sodium thiosulfate and the mixture was stirred for 1 hour while cooling with ice. The resultant precipitate was filtered off, and then washed with methanol. The filtrate was combined with the washings. The resultant mixture 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 20 ml of cold methanol, to thereby obtain the desired product, namely 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. The amount of the desired product was 1.05 g. The yield of the desired product was 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034521
Source datasetuspto-grants-1991_07
ORD IDord-1b4ddd3489a24d83a01223f45bd9ca3d
Source noteuspto-grants-1991_07