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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648756Generated: October 26, 2026

Pyridine → N-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamide

https://huagongshe.com/reaction/648756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiketeneHCID 12661—
Reactant3,4-Dichloro-N-methylanilineHCID 2800931—
SolventTolueneHCID 1140—
ProductN-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamideHCID 13822492—

Reaction Steps

Dissolved in toluene were 3.5 g (0.02 mole) of 3,4-dichloro-N-methylaniline and a catalytic amount of pyridine, followed by a dropwise addition of 1.9 g (0.022 mole) of diketene at 50° C. After completion of the the dropwise addition, the resultant mixture was heated under reflux for 3 hours. The reaction mixture was cooled, and its organic layer was then washed with water, water, a 10% aqueous solution of hydrochloric acid and a 5% aqueous solution of sodium hydrogencarbonate in order. The thus-washed organic solution was dried and concentrated to obtain 3',4'-dichloro-N-methylacetoacetoanilide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736038
Source datasetuspto-grants-1988_04
ORD IDord-8d4a5e6eb18d4834a8e1de7d28d4ce2d
Source noteuspto-grants-1988_04