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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399835Generated: November 2, 2026

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

https://huagongshe.com/reaction/2399835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMonomethyl sulfateHCID 6412—
ReactantTrimethyl borateHCID 8470—
ReactantSulfolaneHCID 31347—
Reactant7-Aminocephalosporanic acidHCID 441328—
Product7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acidHCID 12833023115.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

8.94 g of a methanolic solution of methoxysulfonic acid (prepared as described in Preparation 2) and 2.10 g of trimethyl borate were added to 15 ml of sulfolane. The mixture was cooled to 20° C. 2.74 g of 7-ACA were added to the mixture and the mixture was stirred for 1.5 hours at 20° C. The progress of the reaction was examined by high performance liquid chromatography (HPLC). After completion of the reaction, the reaction mixture was poured over crushed ice and the pH was adjusted to 3.5 by addition of aqueous ammonia. The crystals precipitated were filtered off, washed with water and dried to afford 2.84 g of crude 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. After this, the crude crystals were dissolved in aqueous ammonia in order to adjust the pH to 7. This solution was then applied to an adsorption column (polystyrene type high porous polymer) and the pH of the effluent was adjusted to 3.5 using hydrochloric acid. The crystals precipitated were filtered off, washed with water and dried to give 2.14 g (yield 87%) of the title compound at a high purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451675
Source datasetuspto-grants-1995_09
ORD IDord-ca1d296202d0463c8fbe37888a0e9885
Source noteuspto-grants-1995_09