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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pinacolone | HCID 6416 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-(dimethylamino)benzoate | HCID 25127 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Dimethylaminophenyl)-4,4-dimethylpentane-1,3-dione | HCID 18954482 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05191121 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-a9e0d73991a74236b05a0ce7ac58645c |
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| Source note | uspto-grants-1993_03 |
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