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

HRID 867152

反応式

HRID 867152 の反応式
[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

参加物

8

反応物 4

HCID 1140TolueneHCID 7850Allyl chlorideHCID 14797Potassium HydroxideHCID 913881-(3,3-Dimethylcyclohexyl)ethanone

生成物 3

HCID 64534231-(3,3-Dimethylcyclohexyl)-pent-4-en-1-oneHCID 148178511-[3,3-Dimethyl-1-(prop-2-en-1-yl)cyclohexyl]ethan-1-oneHCID 20317600HCID 20317600、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-1f6a393529744b2383390b63bdc38053
出典データセット
uspto-grants-1978_07
特許番号
US04102928

関連ノート

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