Hydrochloric Acid → 3,4,5-Trimethoxy(4,4-dimethyl-3-oxopentanoyl)benzene

HRID 1613005ノート

反応式

HRID 1613005 の反応式
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([O:17][CH3:18])[C:14]=1[O:15][CH3:16])[C:8]([O:10]C)=O.[CH3:19][C:20](=[O:25])[C:21]([CH3:24])([CH3:23])[CH3:22].Cl>CCCCCC.O1CCCC1>[CH3:18][O:17][C:13]1[CH:12]=[C:7]([C:8](=[O:10])[CH2:19][C:20](=[O:25])[C:21]([CH3:24])([CH3:23])[CH3:22])[CH:6]=[C:5]([O:4][CH3:3])[C:14]=1[O:15][CH3:16]

参加物

7

実験手順

In a 200 ml three-necked flask equipped with a mechanical stirrer, dropping funnel, reflux condenser, and a nitogen-inlet tube, 3.0 gm (75 mmol) of 60% sodium hydride, 10 gm (44.3 mmol) of methyl 3,4,5-trimethoxybenzoate, and 80 ml of anhydrous tetrahydrofuran were mixed with stirring under nitrogen stream, and refluxed with heating while 5.3 gm (53.2 mmol) of pinacolone was added dropwise. Refluxing under heat was continued for 5 hours. After cooling the reaction mixture, 45 ml of 2N hydrochloric acid was added, the mixture was extracted twice with chloroform. The extract was dried over anhydrous sodium sulfate and the solvent was removed by evaporation to give a crude product. Hexane was added to the crude product and insoluble substances were filtered off. The filtrate was concentrated by evaporation, and recrystallization afforded 9.6 gm of the target compound as colorless needles (yield: 74%).

後処理

  1. customIn a 200 ml three-necked flask equipped with a mechanical stirrer
  2. temperaturereflux condenser, and a nitogen-inlet tube
  3. temperaturerefluxed
  4. additionwas added dropwise
  5. temperatureRefluxing
  6. temperatureunder heat
  7. additionwas added
  8. extractionthe mixture was extracted twice with chloroform
  9. dry with materialThe extract was dried over anhydrous sodium sulfate
  10. customthe solvent was removed by evaporation
  11. customto give a crude product
  12. filtrationwere filtered off
  13. concentrationThe filtrate was concentrated by evaporation, and recrystallization

出典と根拠

ORDレコード
ord-af23f4b663924bea9becb7e5ce01a7ac
出典データセット
uspto-grants-1993_03
特許番号
US05191121

反応ノート

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