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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199769Generated: October 30, 2026

Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1199769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBoron trifluorideHCID 6356—
ReactantNitromethaneHCID 6375—
Reactant7-Aminocephalosporanic acidHCID 441328—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 10 ml of nitromethane were added 3.0 g of 7-ACA, 10.0 g of zinc chloride and 3.9 g of a complex of boron trifluoride with methanol (boron trifluoride content: 51%). The mixture was heated at 60° C. for 20 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture were added 30 ml of water and 5 ml of methanol. Then, the mixture was adjusted to pH 8.0 with 28% aqueous ammonia at a temperature of -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 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 obtain the desired product, namely 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. The amount of the desired product was 1.4 g. The yield of the desired product was 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902793
Source datasetuspto-grants-1990_02
ORD IDord-bc48c4182d1e436a905c7f3ddc8ad6cc
Source noteuspto-grants-1990_02