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1-Bromooctadecane → 2-Heneicosanone

HRID 1435099
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HRID 1435099 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

HCID 5298052-Heneicosanone수율 95%

시약·촉매·용매 2

HCID 702Ethanol용매
HCID 962
Water
용매

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온도
95 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-2b68cfa713864002b3a8137d880427a5
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07615672B2

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