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

HRID 1389771
ノート
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反応式

HRID 1389771 の反応式
[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]
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 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

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

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-059ad6b88140418dbc6aec51b76a43c2
出典データセット
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04246267

反応ノート

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