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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224498Generated: October 31, 2026

Dimethylformamide → N-isopropyl-4'-chloro-2-methylacetoacetanilide

https://huagongshe.com/reaction/224498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-isopropyl-4'-chloroacetoacetanilideHCID 20297524—
SolventWaterHCID 962—
ProductN-isopropyl-4'-chloro-2-methylacetoacetanilideHCID 2029752280%

Reaction Steps

A one liter reaction flask equipped with a power stirrer, condener, drying tube, thermometer and nitrogen inlet tube was charged with 48.5 g (0.19 mole) of N-isopropyl-4'-chloroacetoacetanilide and 145 ml of dry dimethylformamide. With efficient stirring in a nitrogen atmosphere, portionwise addition of 7.2 g of 57% sodium hydride in mineral oil (0.17 mole) was completed in one hour (excessive foaming). Methyl iodide (24.1 g, 0.17 mole) was added dropwise and the reaction mixture was stirred for two hours at ambient temperature. The mixture was poured into one liter of cold water and stirred. The organic material was extracted into toluene and the latter was water washed. Most of the toluene was removed on the rotary evaporator. Hexane was added which caused the mass to crystallize. There was obtained 36.4 g (80%) of white material, M.P. 77°-79°. N.M.R. (CDCl3) ∂0.9-1.4 (CH3, 9 protons), 2.0 (0=C--CH3), 2.9-3.2 (CH), 4.7-5.2 (CH, isopropyl), 6.9-7.5. (aromatic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232163
Source datasetuspto-grants-1980_11
ORD IDord-6c275ddd54634c66af47631b8fef69a0
Source noteuspto-grants-1980_11