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Potassium Hydroxide → 2-(o-Tolylthio)-6-(1-propenyl)phenol

HRID 1164105
ノート
印刷プレビュー

反応式

HRID 1164105 の反応式
[C:1]1([CH3:18])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[S:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([CH2:14][CH:15]=[CH2:16])[C:9]=1[OH:17].[OH-].[K+]>CO>[C:1]1([CH3:18])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[S:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([CH:14]=[CH:15][CH3:16])[C:9]=1[OH:17]
参加物反応条件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 14797Potassium HydroxideHCID 130666692-(o-Tolylthio)-6-allylphenol

生成物 1

HCID 544721892-(o-Tolylthio)-6-(1-propenyl)phenol収率 101.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
110 °C

実験手順

A mixture of 2-(o-tolylthio)-6-allylphenol (24 g) and potassium hydroxide (32 g) in methanol (100 ml) was stirred at 110° C. Methanol was distilled off from the mixture under ordinal pressure, and the mixture was stirred at 100° C. for an hour. The reaction mixture was cooled, acidified with conc. hydrochloric acid and extracted with diethyl ether. The extract was washed with water, dried and evaporated under reduced pressure to give oily 2-(o-tolylthio)-6-(1-propenyl)phenol (24.3 g).

後処理

  1. distillationMethanol was distilled off from the mixture under ordinal pressure
  2. stirringthe mixture was stirred at 100° C. for an hour
  3. temperatureThe reaction mixture was cooled
  4. extractionextracted with diethyl ether
  5. washThe extract was washed with water
  6. customdried
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-b8409a1ca364426c9b8b0c2eb35354fc
出典データセット
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04367238

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート