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

HRID 1164105
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HRID 1164105 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 130666692-(o-Tolylthio)-6-allylphenol

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

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온도
110 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-b8409a1ca364426c9b8b0c2eb35354fc
출처 데이터셋
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04367238

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