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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702053Generated: October 31, 2026

Hydrochloric Acid → 7-(2-Methoxyimino-3-oxobutyramido)-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1702053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant7-(2-Methoxyimino-3-oxobutyramido)-3-hydroxycepham-4-carboxylic acidHCID 86738088—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-(2-Methoxyimino-3-oxobutyramido)-3-cephem-4-carboxylic acidHCID 13171252869.6%

Reaction Steps

Trifluoroaceticanhydride (0.2 ml.) and triethylamine (0.12 ml.) were added to a solution of 7-(2-methoxyimino-3-oxobutyramido)-3-hydroxycepham-4-carboxylic acid (syn isomer, 100 mg.) in dry tetrahydrofuran (10 ml.), and allowed to stand at room temperature for 10 minutes. Ethyl acetate (30 ml.) and water (10 ml.) were added to the reaction mixture and adjusted to pH 2 with hydrochloric acid. The ethyl acetate layer was separated, washed with water, dried over magnesium sulfate and then evaporated in vacuo. The residue was crystallized with diethyl ether to give 7-(2-methoxyimino-3-oxobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 66 mg.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379922
Source datasetuspto-grants-1983_04
ORD IDord-36c8acf2b1ab4ca7b89f438d8e46841b
Source noteuspto-grants-1983_04