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

HRID 2416175ノート

反応式

HRID 2416175 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].[O-]CC.[Na+].C1CCCCCCCCCCC1.[CH3:29][C:30]([C@@H:32]1[C:37]([CH3:39])([CH3:38])[CH2:36][CH:35]=[CH:34][C@H:33]1[CH3:40])=[O:31]>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].[CH3:29][C:30]([C:32]1[C:37]([CH3:39])([CH3:38])[CH2:36][CH2:35][CH2:34][C:33]=1[CH3:40])=[O:31]

参加物

7

反応物 4

HCID 9268CyclododecaneHCID 117287Ethanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-HCID 2723922Sodium ethoxideHCID 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, sodium ethoxide (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 130 to 140° 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 34.7%, 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 45.4% and 19.9%, respectively. As a result of calculation, the yield of a mixture of these three methyl ketones was found to be 6.9 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 130 to 140° 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-042dfd045bc146b58ecdff8456de7500
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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