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

HRID 1605131
ノート
印刷プレビュー

反応式

HRID 1605131 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-eaeb01dc512c48c198438fad53d8582f
出典データセット
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03948996

反応ノート

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