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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417709Generated: November 1, 2026

Ethanol → 4-[(2,4-Dichlorophenyl)(hydroxyimino)methyl]-1-piperidinecarboxaldehyde

https://huagongshe.com/reaction/2417709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantAmmonium AcetateHCID 517165—
Reactant4-(2,4-Dichlorobenzoyl)piperidine-1-carbaldehydeHCID 13450895—
SolventWaterHCID 962—
Product4-[(2,4-Dichlorophenyl)(hydroxyimino)methyl]-1-piperidinecarboxaldehydeHCID 8864319914.2%

Reaction Steps

A mixture of 105 g of 4-(2,4-dichlorobenzoyl)-1-formylpiperidine, 70 g of hydroxylamine hydrochloride, 135.0 g of ammonium acetate, 1.05 l of ethanol and 350 ml of water was stirred and heated at 130° for 40 hrs. The reaction mixture was evaporated and 2 l of water was added to the residue. The water was decanted from the oil and oil was washed two times with 500 ml water and then dissolved in about 400 ml dichloromethane. The insoluble material was collected. The dichloromethane extract was washed twice with 600 ml of water and the organic extract was evaporated. Trituration with diisopropyl ether and crystallization from acetone/ether gave 15.6 g (14.2%) of product, mp, 149°-150°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469869
Source datasetuspto-grants-1984_09
ORD IDord-a6cf46e312f9492b916b02016587ee88
Source noteuspto-grants-1984_09