Water → 1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene

HRID 614247ノート

反応式

HRID 614247 の反応式
[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].[CH3:13][S:14][CH2:15][S:16](=[O:18])[CH3:17].CC(C)([O-])C.[K+].O>C(O)(C)(C)C.C(Cl)Cl>[CH3:17][S:16]([C:15]([S:14][CH3:13])=[CH:9][C:8]1[CH:11]=[CH:12][C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[CH:6][CH:7]=1)=[O:18]

参加物

7

反応物 4

HCID 962WaterHCID 99129Methyl (methylsulfinyl)methyl sulfideHCID 577537Benzaldehyde, 4-(2-methylpropyl)-HCID 23665647Potassium tert-butoxide

生成物 1

HCID 545626121-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene収率 87.2%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 6386tert-Butanol溶媒2 回

実験手順

p-Isobutylbenzaldehyde (486 mg) and 450 mg of formaldehyde dimethyl mercaptal S-oxide were dissolved in 1 ml of t-butanol, and 2.0 ml of a 0.608N t-butanol solution of potassium t-butoxide was added. The mixture was stirred at room temperature for 12 hours. Water (0.5 ml) and 50 ml of methylene chloride were added to the reaction mixture. The resulting mixture was dried over anhydrous sodium sulfate. The drying agent and the insoluble matter were removed by filtration, and the filtrate was concentrated under reduced pressure. The oily residue was chromatographed on a silica gel column using methylene chloride as an eluant to afford 701 mg of 1-methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene in a yield of 87%. Samples for analysis were obtained by simple distillation of this product (at a bath temperature of 160° to 170° C./0.02 mmHg).

後処理

  1. dry with materialThe resulting mixture was dried over anhydrous sodium sulfate
  2. customThe drying agent and the insoluble matter were removed by filtration
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe oily residue was chromatographed on a silica gel column

出典と根拠

ORDレコード
ord-7b4a58ef82c649e5ab1840a140114152
出典データセット
uspto-grants-1979_03
特許番号
US04144248

反応ノート

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