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

HRID 1605140
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반응식

HRID 1605140 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

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

생성물 1

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

시약·촉매·용매 2

HCID 280
Carbon Dioxide
용매
2회
HCID 3283Diethyl Ether용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-fd3dbbd02e2d447392885f38ae5c7a71
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03948996

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