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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768678Generated: November 2, 2026

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

https://huagongshe.com/reaction/1768678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydrideHCID 62714—
ReactantBenzoyl chloride, 4-(2,2-dimethyl-1-oxopropyl)-HCID 11806342—
Reactant4-(2,2-Dimethylpropanoyl)-N-methoxybenzamideHCID 15232841—
SolventTolueneHCID 1140—
Product4-(2,2-dimethyl-1-oxopropyl)-N-methoxy-N-[4-(2,2-dimethyl-1-oxopropyl)-benzoyl]-benzamideHCID 15232846—

Reaction Steps

To a suspension of 0.64 grams(80 mmol) of lithium hydride in 150 ml of toluene, 9.4 grams (40 mmol) of solid 4- (2,2-dimethyl-1-oxopropyl)-N-methoxybenzamide is added portion-wise at room temperature and stirred for 1 1/2 hours. To this suspension, 9.93 grams (44.2 mmol) of 4- (2,2-dimethyl-1-oxopropyl)-benzoyl chloride dissolved in 50 ml of toluene is added at room temperature. The reaction mixture is stirred for 60 hours and then heated at 65°-70° C. for 22 hours. The mixture is poured into 250 ml. of cold pH7 phosphate buffer under nitrogen and the aqueous phase is then separated and extracted twice with t-butyl methyl ether. The organic layers are washed with dilute sodium bicarbonate solution and after drying over magnesium sulfate, the organic phase is evaporated to dryness. The crude product is crystallized from t-butyl methyl ether/heptane and then recrystallized 3 times from toluene/heptane. After each recrystallization, the nugget-like crystals, enriched in the desired product, are physically separated from the powdery crystals to yield the title compound (m.p. 103°-105 ° C. ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378728
Source datasetuspto-grants-1995_01
ORD IDord-9072a7f835a54783a08466a705f3cef6
Source noteuspto-grants-1995_01