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Hydroquinone → 7-Methylthio-3,7-dimethyloctan-1-ol

HRID 1605140
ノート
印刷プレビュー

反応式

HRID 1605140 の反応式
[CH3:1][C:2](=[CH:4][CH2:5][CH2:6][CH:7]([CH2:9][CH2:10][OH:11])[CH3:8])[CH3:3].C1(C)C=C[C:15]([S:18](O)(=O)=O)=CC=1.C1(C=CC(O)=CC=1)O.CS.[OH-].[Na+]>C(=O)=O.CCOCC>[CH3:15][S:18][C:2]([CH3:3])([CH3:1])[CH2:4][CH2:5][CH2:6][CH:7]([CH3:8])[CH2:9][CH2:10][OH:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 785HydroquinoneHCID 878MethanethiolHCID 6101p-Toluenesulfonic acidHCID 8842CitronellolHCID 14798Sodium Hydroxide

生成物 1

HCID 215493537-Methylthio-3,7-dimethyloctan-1-ol

試薬・触媒・溶媒 2

HCID 280
Carbon Dioxide
溶媒
2 回
HCID 3283Diethyl Ether溶媒

実験手順

A mixture of 4 g. of citronellol (3,7-dimethyloct-6-en-1-ol), 0.490 g. of p-toluenesulfonic acid and 0.290 g. of hydroquinone is placed in a stainles steel screw cap bomb having an internal volume of 45 ml. The bomb is cooled in dry ice. Methyl mercaptan (9 g.) is introduced directly into the bomb through the valve head. The bomb is sealed, left overnight at room temperature and then heated to 220° in an oil bath for about 72 hours. After cooling in dry ice, the bomb valve is opened and the reaction mixture is carefully poured into 5% aqueous sodium hydroxide solution. Ether is added and the organic layer is separated, washed with 5% NaOH, 5% HCl and water, dired over calcium sulfate and concentrated with vacuo to yield 7-methylthio-3,7-dimethyloctan-1-ol.

後処理

  1. additionA mixture of 4 g
  2. customscrew cap bomb
  3. customThe bomb is sealed
  4. temperatureheated to 220° in an oil bath for about 72 hours
  5. customthe organic layer is separated
  6. washwashed with 5% NaOH, 5% HCl and water
  7. concentrationconcentrated with vacuo

出典と根拠

ORDレコード
ord-fd3dbbd02e2d447392885f38ae5c7a71
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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