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

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.

1. customInto a 100 ml three-necked flask equipped with a stirrer, a dropping funnel, a reflux condenser, and a nitogen-inlet tube
2. temperatureheated
3. temperatureunder refluxing
4. temperaturethe mixture was heated
5. temperatureAfter cooling
6. extractionthe organic layer was extracted twice with chloroform
7. washThe extract was thoroughly washed with water
8. dry with materialdried over anhydrous magnesium sulfate
9. customThe solvent was removed by evaporation
10. customto obtain an yellow oil
11. distillationThe oily substance was submitted to the Kugelrohr distillation 150° C., 1 mmHg
12. customcrystallized from hexane

ORDレコード

ord-a9e0d73991a74236b05a0ce7ac58645c

出典データセット

uspto-grants-1993_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05191121