Sulfuric Acid → 3-(3-Oxobut-1-enyl)-2,4,4-trimethylcyclohex-2-en-1-one

HRID 1106093

반응식

HRID 1106093 반응식
[CH3:1][C:2]1[CH:7]([OH:8])[CH2:6][CH2:5][C:4]([CH3:10])([CH3:9])[C:3]=1[CH:11]=[CH:12][C:13](=[O:15])[CH3:14].O.O.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[Na+].[Na+].S(=O)(=O)(O)O>CCOCC>[CH3:1][C:2]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]([CH3:9])([CH3:10])[C:3]=1[CH:11]=[CH:12][C:13](=[O:15])[CH3:14]

참가 물질

5

반응 조건

온도
5 °C

실험 절차

To a solution, pre-cooled to 0° C., of 140 g (0.068 mol) of 4-(2,6,6-trimethyl-3-hydroxy-cyclohex-1-en-1-yl)-but-3-en-2-one in 500 ml of ether are added dropwise over a period of 10 minutes 700 ml of an aqueous solution, cooled to 0° C., of 202.6 g of sodium dichromate dihydrate and 186 g of concentrated sulphuric acid with intensive cooling and good stirring so that a temperature of 5° C. is not exceeded. The mixture is then stirred for a further 5 minutes at 5° C., treated with 500 ml of ether, the ether phase is washed three times with water, three times with soda solution and again three times with water, dried over sodium sulphate and concentrated. Distillation of the resulting 125 g of crude product over a 10 cm Widmer column gave 103 g of more than 94% pure 4-(2,6,6-trimethyl-3-oxo-cyclohex-1-en-1-yl)-but- 3-en-2-one of boiling point 109°-110° C./0.05 mm Hg; melting point 50°-51° C.

후처리

  1. temperaturewith intensive cooling
  2. stirringThe mixture is then stirred for a further 5 minutes at 5° C.
  3. washthe ether phase is washed three times with water, three times with soda solution and again three times with water
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated
  6. distillationDistillation of the resulting 125 g of crude product over a 10 cm Widmer column

출처 및 근거

ORD 기록
ord-f6f2645b82d4426cbf7dd5593ee9b3f5
출처 데이터셋
uspto-grants-1982_01
특허 번호
US04311718

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