Toluene → 1-(3,3-Dimethylcyclohexyl)-pent-4-en-1-one

HRID 867152

반응식

HRID 867152 반응식
[C:1]([CH:4]1[CH2:9][CH2:8][CH2:7][C:6]([CH3:11])([CH3:10])[CH2:5]1)(=[O:3])[CH3:2].[OH-].[K+].[C:14]1(C)[CH:19]=CC=C[CH:15]=1.[CH2:21](Cl)[CH:22]=[CH2:23]>O>[C:1]([CH2:4][CH2:5][C:6]([CH3:10])([CH3:11])[CH2:7][CH2:8][CH3:9])(=[O:3])[CH3:2].[C:1]([C:4]1([CH2:19][CH:14]=[CH2:15])[CH2:9][CH2:8][CH2:7][C:6]([CH3:11])([CH3:10])[CH2:5]1)(=[O:3])[CH3:2].[CH3:10][C:6]1([CH3:11])[CH2:7][CH2:8][CH2:9][CH:4]([C:1](=[O:3])[CH2:2][CH2:23][CH:22]=[CH2:21])[CH2:5]1

참가 물질

8

실험 절차

A slurry of 1-acetyl-3,3-dimethylcyclohexane (156 grams, 1 mole), potassium hydroxide (86 grams, 1.5 moles), and toluene (300 ml) is heated to reflux. Allyl chloride (114 grams, 1.5 moles) is added to the thickened reaction mass whereupon the mass becomes more fluid. The mixture is heated at reflux for 61/2 hours. At the end of this period, the reaction mass is cooled to room temperature, and 500 ml of water is added thereto. The aqueous layer is discarded, and the organic layer is distilled to afford 74 grams of recovered 1-acetyl-3,3-dimethyl hexane, 53 grams of 1-acetyl-3,3-dimethyl-1-(2-propenyl) cyclohexane, and 35 grams of 3,3-dimethyl-1-(4-pentenoyl) cyclohexane.

후처리

  1. temperatureThe mixture is heated
  2. temperatureat reflux for 61/2 hours
  3. distillationthe organic layer is distilled

출처 및 근거

ORD 기록
ord-1f6a393529744b2383390b63bdc38053
출처 데이터셋
uspto-grants-1978_07
특허 번호
US04102928

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