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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164423Generated: November 2, 2026

Pyridine → HCID 131712939, compound

https://huagongshe.com/reaction/1164423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 70464109HCID 70464109—
SolventDimethylformamideHCID 6228—
ProductHCID 131712939HCID 13171293979.2%

Reaction Steps

In dimethylformamide (5 ml) are dissolved 2,2,2-trichloroethyl 3-methyl-7-oxo-3-cephem-4-carboxylate (691 mg) and hydroxylamine hydrochloride (139 mg), followed by addition of pyridine (162 μl) and methylene chloride (10 ml). The mixture is refluxed in a Dean-Stark trap packed with Molecular Sieve 3A for 45 minutes. The reaction mixture is concentrated under reduced pressure and the residue is dissolved in ethyl acetate. The resultant solution is washed with water and aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residual oil is subjected to silica gel (20 g) column chromatography and elution is carried out with 5-13% ethyl acetatehexane to give 2,2,2-trichloroethyl 7-hydroxyimino-3-methyl-3-cephem-4-carboxylate as an oil (570 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369312
Source datasetuspto-grants-1983_01
ORD IDord-85c60d7ea8a1499aa64cbc431d007ed6
Source noteuspto-grants-1983_01