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Iodine → 6,6-Dimethyl-1-heptene

HRID 1904417
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HRID 1904417 반응식
[CH3:1][C:2]([CH3:5])([CH3:4])[CH3:3].[Mg].II.Br[CH2:10][CH2:11][CH:12]=[CH2:13]>O1CCCC1>[CH3:1][C:2]([CH3:5])([CH3:4])[CH2:3][CH2:13][CH2:12][CH:11]=[CH2:10]
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참가 물질

6

반응물 4

HCID 807IodineHCID 10041NeopentaneHCID 21241Homoallyl bromideHCID 5462224Magnesium

생성물 1

HCID 144593876,6-Dimethyl-1-heptene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2,2-Dimethylpropane (15.1 g, 0.10 mol) in dry tetrahydrofuran (80 ml) was added dropwise to a mixture of magnesium turnings (2.43 g, 0.10 mol) in dry tetrahydrofuran (20 ml) containing a single crystal of iodine, at such a rate so as to maintain the solvent at reflux. The resulting solution was allowed to cool to room temperature and decanted from the residual magnesium under nitrogen into a fresh flask. The solution was diluted with dry tetrahydrofuran (150 ml), cooled to -20° C. under an atmosphere of nitrogen treated with cuprous bromide dimethyl sulphide complex and stirred for 20 minutes. The resulting solution was then treated with 4-bromo-1-butene (13.5 g, 0.10 mol) and stirred at -20° C. for 16 hours and then at 20° C. for 4 hours. The reaction mixture as quenched with saturated aqueous ammonium chloride solution (10 ml), diluted with ether (200 ml) and washed with an aqueous solution of ammonia (2×200 ml of 10%). The solution was dried over sodium sulfate and distilled at atmospheric pressure to yield 6,6-dimethyl- 1-heptene as a colourless oil, having a boiling point of 120°-125° C., and the following structural characteristics:

후처리

  1. temperatureat such a rate so as to maintain the solvent
  2. temperatureat reflux
  3. customdecanted from the residual magnesium under nitrogen into a fresh flask
  4. additionThe solution was diluted with dry tetrahydrofuran (150 ml)
  5. temperaturecooled to -20° C. under an atmosphere of nitrogen
  6. additiontreated with cuprous bromide dimethyl sulphide complex
  7. stirringstirred at -20° C. for 16 hours
  8. waitat 20° C. for 4 hours
  9. customThe reaction mixture as quenched with saturated aqueous ammonium chloride solution (10 ml)
  10. additiondiluted with ether (200 ml)
  11. washwashed with an aqueous solution of ammonia (2×200 ml of 10%)
  12. dry with materialThe solution was dried over sodium sulfate
  13. distillationdistilled at atmospheric pressure

출처 및 근거

ORD 기록
ord-bfdb595376384f2ba24e31c6ab9ed302
출처 데이터셋
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04837333

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