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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613014Generated: October 25, 2026

Hydrochloric Acid → 1-(4-Dimethylaminophenyl)-4,4-dimethylpentane-1,3-dione

https://huagongshe.com/reaction/1613014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPinacoloneHCID 6416—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-(dimethylamino)benzoateHCID 25127—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Dimethylaminophenyl)-4,4-dimethylpentane-1,3-dioneHCID 1895448270%

Reaction Steps

Into a 100 ml three-necked flask equipped with a stirrer, a dropping funnel, a reflux condenser, and a nitogen-inlet tube, were charged 2.08 gm (31 mmol) of 60% sodium hydride and 5.0 gm (26 mmol) of ethyl 4-dimethylaminobenzoate. The mixture was dispersed in 40 ml of tetrahydrofuran and heated under refluxing. To the mixture was dropwise added 3.0 gm (30 mmol) of pinacolone and the mixture was heated with stirring for 3 hours. After cooling, 50 ml of 1N hydrochloric acid was added to the reaction mixture, and the organic layer was extracted twice with chloroform. The extract was thoroughly washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by evaporation to obtain an yellow oil. The oily substance was submitted to the Kugelrohr distillation 150° C., 1 mmHg, and crystallized from hexane to give 4.5 gm (yield: 70%) of yellow solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05191121
Source datasetuspto-grants-1993_03
ORD IDord-a9e0d73991a74236b05a0ce7ac58645c
Source noteuspto-grants-1993_03