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Methyl iodide → 1,1-Dimethoxy-7-methylthio-3,7-dimethyloctane

HRID 1605131
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반응식

HRID 1605131 반응식
[CH3:1][O:2][CH:3]([O:14][CH3:15])[CH2:4][CH:5]([CH3:13])[CH2:6][CH2:7][CH2:8][C:9]([SH:12])([CH3:11])[CH3:10].[CH3:16][O-].[Na+].CI>CO>[CH3:1][O:2][CH:3]([O:14][CH3:15])[CH2:4][CH:5]([CH3:13])[CH2:6][CH2:7][CH2:8][C:9]([S:12][CH3:16])([CH3:10])[CH3:11]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 10942334Sodium MethoxideHCID 215493991,1-Dimethoxy-7-mercapto-3,7-dimethyloctane

생성물 1

HCID 215493561,1-Dimethoxy-7-methylthio-3,7-dimethyloctane

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 10 g. of 1,1-dimethoxy-7-mercapto-3,7-dimethyloctane, one equiv. of sodium methoxide and 100 ml. of methanol is added 1.5 equivalents of methyl iodide. The mixture is stirred for 2 hours at room temperature and then refluxed for 2 hours. After cooling to room temperature, solvent is removed by evaporation and the residue taken up in ether. The ether solution is washed with water, dried and evaporated under reduced pressure to give 1,1-dimethoxy-7-methylthio-3,7-dimethyloctane which can be purified by chromatography or distillation.

후처리

  1. additionTo a mixture of 10 g
  2. temperaturerefluxed for 2 hours
  3. temperatureAfter cooling to room temperature
  4. customsolvent is removed by evaporation
  5. washThe ether solution is washed with water
  6. customdried
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-eaeb01dc512c48c198438fad53d8582f
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03948996

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