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2,6-Dimethylthiophenol → 2-[(2,6-Dimethylphenyl)sulfanyl]ethan-1-ol

HRID 1389771
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HRID 1389771 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[SH:9].Cl[CH:11]([OH:13])[CH3:12]>[OH-].[Na+].O>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[S:9][CH2:12][CH2:11][OH:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 610452,6-DimethylthiophenolHCID 126390351-Chloroethan-1-ol

생성물 1

HCID 27586362-[(2,6-Dimethylphenyl)sulfanyl]ethan-1-ol수율 95%

시약·촉매·용매 2

HCID 962Water용매HCID 14798Sodium Hydroxide용매

실험 절차

35 g. 2,6-dimethyl thiophenol are dissolved in a solution of 15.6 g sodium hydroxide in 210 ml water, under stirring and inert atmospher. After complete dissolution 34 g chloro ethanol are added portionwise thereto and the milky suspension is thereafter heated to reflux for one hour. The mixture reverts to room temperature and is extracted three times with ester to isolate the thus formed oily product. The ethereous solutions are washed with water, dried on sodium sulphate, filtered and evaporated off. 2-(2,6-dimethyl phenylthio) 1-hydroxy ethane is obtained with a yield of 95%. It is further used for the next step without any purification

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후처리

  1. additionare added portionwise
  2. temperaturethe milky suspension is thereafter heated
  3. temperatureto reflux for one hour
  4. customreverts to room temperature
  5. extractionis extracted three times with ester
  6. customto isolate the thus formed oily product
  7. washThe ethereous solutions are washed with water
  8. customdried on sodium sulphate
  9. filtrationfiltered
  10. customevaporated off

출처 및 근거

ORD 기록
ord-059ad6b88140418dbc6aec51b76a43c2
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04246267

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