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Iodine → 5,9-Dimethylpentadecane

HRID 344629
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HRID 344629 반응식
[Mg].II.Cl[CH2:5][CH:6]([CH3:16])[CH2:7][CH2:8][CH2:9][CH:10]([CH3:15])[CH2:11][CH2:12][CH2:13][CH3:14].Br[CH2:18][CH2:19]Br.Br[CH2:22][CH2:23][CH2:24]CC>O1CCCC1.[Li+].[Li+].[Cl-].[Cl-].[Cl-].[Cl-].[Cu+2]>[CH3:16][CH:6]([CH2:7][CH2:8][CH2:9][CH:10]([CH3:15])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:18][CH3:19])[CH2:5][CH2:22][CH2:23][CH3:24]
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8

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HCID 807IodineHCID 78391,2-DibromoethaneHCID 80571-BromopentaneHCID 5462224MagnesiumHCID 142782011-Chloro-2,6-dimethyldecane

생성물 1

HCID 142782025,9-Dimethylpentadecane수율 64.8%

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
4회
HCID 193501Copper;dilithium;tetrachloride용매

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온도
-20 °C

실험 절차

Magnesium (0.54 g, 22.2 mmol) is etched with iodine and 0.5 ml of a solution of 93% 1-chloro-2,6-dimethyldecane (4.5 g, 20.7 mmol) in tetrahydrofuran (4 ml) is added at 60° C. After the reaction has been started by addition of a drop of 1,2-dibromoethane the rest of the solution is added dropwise. The mixture is diluted with tetrahydrofuran (4 ml) and stirred under reflux for 2.5 h, then cooled to -20° C. 1-Bromopentane (3.8 g, 25 mmol) in tetrahydrofurane (4 ml) and 0.5M dilithium tetrachlorocuprate in tetrahydrofuran (3 ml) are added, and the mixture is stirred at -20° C. for 2 h, at 0° C. for 2 h, and at room temperature overnight. Subsequent treatment with ammonium chloride solution and distillation gives 3.22 g of 5,9-dimethylpentadecane, a yield of 64.8% based on the amount of C12 -alkyl chloride.

후처리

  1. additionis added at 60° C
  2. additionis added dropwise
  3. temperatureunder reflux for 2.5 h
  4. stirringthe mixture is stirred at -20° C. for 2 h, at 0° C. for 2 h
  5. customat room temperature
  6. customovernight
  7. distillationSubsequent treatment with ammonium chloride solution and distillation

출처 및 근거

ORD 기록
ord-6f9de3b839674cb88ef2d2a26a5e8641
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05053223

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