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1-Bromooctadecane → 2-Heneicosanone

HRID 1435099
ノート
印刷プレビュー

反応式

HRID 1435099 の反応式
[CH3:1][C:2](=O)[CH2:3][C:4](=[O:6])[CH3:5].Br[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]CC.C1OCCOCCOCCOCCOCCOC1.C(=O)([O-])[O-].[K+].[K+]>O.C(O)C>[CH3:5][C:4](=[O:6])[CH2:3][CH2:2][CH2:1][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH3:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 82181-BromooctadecaneHCID 11430Potassium CarbonateHCID 2855718-Crown-6HCID 31261Acetylacetone

生成物 1

HCID 5298052-Heneicosanone収率 95%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 962
Water
溶媒

反応条件

温度
95 °C

実験手順

To a 2 L two-necked round bottom flask equipped with water condenser, calcium chloride guard tube and mechanical stirrer, 100 g of 2,4-pentanedione, 600 g of 1-bromooctadecane, 10 g of 18-crown-6, anhydrous potassium carbonate 125 g and 550 ml of absolute ethanol were added with stirring. The mixture was refluxed at 95° C. with continuous stirring for 24 hrs, after refluxing at the said temperature, the mixture was cooled to ambient temperature (25° C.), 550 ml of water was added to it and the 2-heneicosanone was extracted with dichloromethane from the mixture. On distillation of dichloromethane, 2-heneicosanone was obtained.

後処理

  1. customTo a 2 L two-necked round bottom flask equipped with water condenser, calcium chloride guard tube and mechanical stirrer
  2. stirringwith continuous stirring for 24 hrs
  3. temperatureafter refluxing at the said temperature
  4. additionwas added to it
  5. extractionthe 2-heneicosanone was extracted with dichloromethane from the mixture
  6. distillationOn distillation of dichloromethane

出典と根拠

ORDレコード
ord-2b68cfa713864002b3a8137d880427a5
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07615672B2

反応ノート

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