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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972487Generated: October 29, 2026

O-Methylhydroxylamine hydrochloride → HCID 131710493, compound

https://huagongshe.com/reaction/972487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 88819529HCID 88819529—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131710493HCID 131710493—

Reaction Steps

To a solution of 3-formyl-7β-(2-thienylacetamido)-3-cephem-4-carboxylic acid (35 mg) in tetrahydrofuran (3 ml) is added a solution of O-methylhydroxylamine hydrochloride (13 mg) in water (1.5 ml), and the mixture is left standing for 24 hours. After evaporation of the tetrahydrofuran at room temperature, the separated yellow oil is extracted with ethyl acetate. The extract solution is washed with water, dried and evaporated to leave pale yellow foam which gives crystals of 3-methoxyiminomethyl-7β-(2-thienylacetamido)-3-cephem-4-carboxylic acid (37 mg; nearly quantitative yield) by recrystallization from ether and ethyl acetate. m.p. 186°-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053469
Source datasetuspto-grants-1977_10
ORD IDord-2540aea182704a018bec6cb7ca7ef04e
Source noteuspto-grants-1977_10