Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47081Generated: October 26, 2026

Water → Di-(4-chlorophenyl)methyleneamino-oxyacetamide

https://huagongshe.com/reaction/47081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetamideHCID 6580—
ReactantSodium hydrideHCID 24758—
Reactant4,4'-Dichlorobenzophenone oximeHCID 74389—
SolventDimethylformamideHCID 6228—
ProductDi-(4-chlorophenyl)methyleneamino-oxyacetamideHCID 1294246435.4%

Reaction Steps

Sodium hydride (0.5 g., 50% w/w suspension in mineral oil) was added gradually to a stirred solution of 4,4'-dichlorobenzophenone oxime (2.6 g.) in dry dimethylformamide (20 ml.) keeping the temperature below 30° C. After 30 minutes, chloroacetamide (0.9 g.) was added to the stirred solution keeping the temperature below 30° C. After 16 hours stirring at ambient temperature the mixture was poured into water (100 ml.) and the subsequent mixture extracted with ether. The combined extract was washed with water, dried (MgSO4) and evaporated. The residue (2.5 g.) was added to a column of dry chromatographic silica-gel [300 g., previously deactivated by addition of 10% w/w water and then equilibrated with 10% v/w of a mixture of toluene and acetone (10:1 v/w)]. The column was then eluted with the same mixture of toluene and acetone to give, after evaporation of solvent, a solid residue (1.5 g.). The solid was recrystallised from ethyl acetate/petrol giving di-(4-chlorophenyl)methyleneamino-oxyacetamide m.p. 141°-142° C. (1.1 g.) in 34% overall yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04176194
Source datasetuspto-grants-1979_11
ORD IDord-4be65f9271554c169cb8663e62cfe682
Source noteuspto-grants-1979_11