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Salicyl Alcohol → 2-[(Ethylsulfanyl)methyl]phenol

HRID 2198592
ノート
印刷プレビュー

反応式

HRID 2198592 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9].[CH2:10]([SH:12])[CH3:11]>ClC1C=CC=CC=1Cl>[CH2:10]([S:12][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5146Salicyl AlcoholHCID 6343Ethanethiol

生成物 1

HCID 5221672-[(Ethylsulfanyl)methyl]phenol収率 87%

試薬・触媒・溶媒 1

HCID 72391,2-Dichlorobenzene溶媒

実験手順

A mixture of 49.6 g (0.4 mol) of 2-hydroxymethyl-phenol, 24.8 g (0.4 mol) of ethylmercaptan and 200 ml of o-dichlorobenzene was heated in a flask equipped with a stirrer and a reflux condenser, under normal pressure, and starting from room temperature, in such a way that there was always a moderate reflux and that the final temperature in the flask did not exceed about 125° C. In total, the mixture was heated under reflux for about 20 hours. Thereafter, working up by distillation gave 2-ethylthiomethyl-phenol in a yield of 87% of theory. The o-dichlorobenzene distilled off could be re-used in a subsequent batch.

後処理

  1. temperaturewas heated in a flask
  2. customequipped with a stirrer and a reflux condenser, under normal pressure
  3. customstarting from room temperature
  4. temperaturea moderate reflux
  5. customdid not exceed about 125° C
  6. temperatureIn total, the mixture was heated
  7. temperatureunder reflux for about 20 hours
  8. distillationThereafter, working up by distillation

出典と根拠

ORDレコード
ord-85871db35598409f84503505060a132e
出典データセット
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04358616

反応ノート

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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