Cyclododecane → 1-(2,6,6-Trimethyl-1-cyclohexen-1-yl)ethanone

HRID 2416176ノート

反応式

HRID 2416176 の反応式
[CH3:1][C:2]([CH:4]1[C:9]([CH3:11])([CH3:10])[CH2:8][CH:7]=[CH:6][CH:5]1[CH3:12])=[O:3].[OH-].[K+].C1CCCCCCCCCCC1.[CH3:27][C:28]([C@@H:30]1[C:35]([CH3:37])([CH3:36])[CH2:34][CH:33]=[CH:32][C@H:31]1[CH3:38])=[O:29]>CS(C)=O>[CH3:1][C:2]([CH:4]1[C:9]([CH3:11])([CH3:10])[CH2:8][CH2:7][CH:6]=[C:5]1[CH3:12])=[O:3].[CH3:27][C:28]([C:30]1[C:35]([CH3:37])([CH3:36])[CH2:34][CH2:33][CH2:32][C:31]=1[CH3:38])=[O:29]

参加物

7

反応物 4

HCID 9268CyclododecaneHCID 14797Potassium HydroxideHCID 117287Ethanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-HCID 54437493Trans-4-Acetyl-3,5,5-Trimethylcyclohexene

生成物 2

HCID 5393161-(2,6,6-Trimethyl-1-cyclohexen-1-yl)ethanoneHCID 157476822,6,6-Trimethyl-2-cyclohexenyl methyl ketone

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

In a 100-ml four-necked flask equipped with a thermometer, a condenser and a stirrer, placed were 2,6,6-trimethyl-3-cyclohexenyl methyl ketone (10 g) synthesized in Referential Example 1, potassium hydroxide (2.5 g), dimethyl sulfoxide (30 ml) and, as an internal standard substance for the analysis by gas chromatography, cyclododecane (3 g). They were reacted at 170 to 190° C. for 6 hours. The reaction mixture was treated in an usual manner. Analysis by gas chromatography showed that the content of trans-2,6,6-trimethyl-3-cyclohexenyl methyl ketone was 67.5%, while those of 2,6,6-trimethyl-2-cyclohexenyl methyl ketone and 2,6,6-trimethyl-1-cyclohexenyl methyl ketone produced by the above reaction were 20.1% and 12.4%, respectively. As a result of calculation, the yield of a mixture of these three methyl ketones was found to be 4.3 g.

後処理

  1. customIn a 100-ml four-necked flask equipped with a thermometer, a condenser and a stirrer
  2. customThey were reacted at 170 to 190° C. for 6 hours
  3. additionThe reaction mixture was treated in an usual manner

出典と根拠

ORDレコード
ord-949eda96cd314b4885a4d65ef6ad8964
出典データセット
uspto-grants-2004_11
特許番号
US06822121B2

反応ノート

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