Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370889Generated: October 30, 2026

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

https://huagongshe.com/reaction/370889

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 numberUS04528376
Source datasetuspto-grants-1985_07
ORD IDord-2429b578ad21457bad7a2cbb428b98c0
Source noteuspto-grants-1985_07