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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979784Generated: October 29, 2026

Hydrochloric Acid → 3-Methoxymethyl-7-phenoxyacetamido-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1979784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCalcium ChlorideHCID 5284359—
ReactantSodium 3-acetoxymethyl-7-phenoxyacetamido-3-cephem-4-carboxylateHCID 23673564—
SolventMethanolHCID 887—
Product3-Methoxymethyl-7-phenoxyacetamido-3-cephem-4-carboxylic acidHCID 1591768480.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

10 g of sodium 3-acetoxymethyl-7-phenoxyacetamido-3-cephem-4-carboxylate were dissolved in 100 ml of a 67% v/v aqueous methanol solution. 100 g of anhydrous calcium chloride were added to the solution, and then the mixture was stirred at 70° C. for 45 minutes. At the end of this time, 100 ml of ice-water, followed by 10 ml of 1N hydrochloric acid, were added to the reaction mixture. The reaction mixture was then extracted three times, each time with 100 ml of ethyl acetate. The extracts were combined, washed with an aqueous solution of sodium chloride and then extracted with two 50 ml portions of a 10% w/v aqueous solution of dipotassium phosphate. The extracts were combined, washed with a small amount of ethyl acetate and then acidified by the addition of a saturated aqueous solution of potassium hydrogen sulphate. The mixture was then extracted twice, each time with 100 ml of ethyl acetate. The ethyl acetate extracts were combined, washed with an aqueous solution of sodium chloride, dehydrated by the addition of anhydrous magnesium sulphate and then concentrated by evaporation under reduced pressure, to give 7.15 g of 3-methoxymethyl-7-phenoxyacetamido-3-cephem-4-carboxylic acid, in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482710
Source datasetuspto-grants-1984_11
ORD IDord-33fd2f9dca0e45dcad8a2198f83f9a5b
Source noteuspto-grants-1984_11