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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463402Generated: October 29, 2026

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

https://huagongshe.com/reaction/463402

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 numberUS04518774
Source datasetuspto-grants-1985_05
ORD IDord-733abb4717f84a9c9736a19ec86e10b5
Source noteuspto-grants-1985_05