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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199766Generated: November 1, 2026

Sodium Sulfide → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1199766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
ReactantBismuth trichlorideHCID 24591—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventNitromethaneHCID 6375—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023—

Reaction Conditions

Temperature30 °C

Reaction Steps

To 10 ml of nitromethane were added 2.72 g of 7-ACA, 2.2 g of methanol, 9.0 g of bismuth trichloride and 5.9 g of ferric chloride. The mixture was heated at 30° C. for 160 min to advance a reaction After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture was added 50 ml of water. Then, the mixture was adjusted to pH 1 with sodium bicarbonate and, then, further adjusted to pH 7.5 with sodium sulfide while cooling on ice. 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. To the mixture was added 50 ml of methanol, and the mixture was allowed to stand at 5° C. for 10 hours, thereby to 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 1.37 g. The yield of the desired product was 56 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902793
Source datasetuspto-grants-1990_02
ORD IDord-b5e58011fe33457b8b907c110b197fe1
Source noteuspto-grants-1990_02