Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199757Generated: November 2, 2026

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

https://huagongshe.com/reaction/1199757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium SulfideHCID 14804—
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, 11.2 g of ferric chloride and 2.1 g of methanol. The mixture was heated at 30° C. for 40 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 50 ml of water. Then, the mixture was adjusted to pH 1.0 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 7 with 1N HCl and applied to a column packed with HP-20 (a packing material for reversed phase adsorption chromatography manufactured and sold by Mitsubishi Chemical Industries, Ltd., Japan). Then, the elution was conducted using water as an eluent, thereby to obtain an eluate. Then, 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 1.02 g. The yield of the desired product was 42 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902793
Source datasetuspto-grants-1990_02
ORD IDord-50561a89d3e040eb933070f4fb983faa
Source noteuspto-grants-1990_02