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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768669Generated: November 1, 2026

Potassium hydride → 4-(2,2-dimethyl-1-oxopropyl)-N-[4-(2,2-dimethyl-1-oxopropyl)-benzoyl]benzamide

https://huagongshe.com/reaction/1768669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
Reactant4-(2,2-Dimethyl-1-oxopropyl)-benzamideHCID 10536234—
ReactantBenzoyl chloride, 4-(2,2-dimethyl-1-oxopropyl)-HCID 11806342—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(2,2-dimethyl-1-oxopropyl)-N-[4-(2,2-dimethyl-1-oxopropyl)-benzoyl]benzamideHCID 9800724—

Reaction Conditions

Temperature0 °C

Reaction Steps

4.2 grams (20.5 mmoles) of 4-(2,2-dimethyl-1-oxopropyl) benzamide is dissolved in 100 milliliters of dry tetrahydrofuran. The solution is cooled to 0° C., and 3.7 grams (22.6 mmoles) of potassium hydride (from a 24.5% mixture in mineral oil) which has been washed free of oil with hexane, is added. After hydrogen evolution has ceased, (approximately 2 hours), a solution of 4.6 grams (20.5 mmoles) of 4-(2,2-dimethyl-1-oxopropyl)-benzoyl chloride in 20 milliliters of dry tetrahydrofuran is added dropwise at 0° C. When addition is complete, the reaction mixture is concentrated in vacuo, and the residue is then dissolved in methylene dichloride and filtered to remove solids. The filtrate is purified by flash chromatography (3 inch column and 0.3% then 1% methanol/methylene chloride to elute) and crystallized from diethyl ether to yield the title product (m.p. 131°-132° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378728
Source datasetuspto-grants-1995_01
ORD IDord-c881b126b3004ca1929902fc5ee5105c
Source noteuspto-grants-1995_01