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Benzyl Alcohol → 4-(Benzylthio)phenol

HRID 614040
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인쇄 미리보기

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HRID 614040 반응식
[SH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH2:9](O)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C1(C)C(S(O)(=O)=O)=CC=CC=1.C1C=CC=CC=1>[CH2:9]([S:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 244Benzyl AlcoholHCID 2401474-Mercaptophenol

생성물 1

HCID 50183854-(Benzylthio)phenol

시약·촉매·용매 2

HCID 69252-Methylbenzenesulfonic acid촉매HCID 241Benzene용매

실험 절차

4-(Benzylthio)phenol was prepared as follows. Seventy grams of 4-mercaptophenol, 30 drops of toluene sulfonic acid and 100 milliliters of benzene were placed in a flask. Eighty-three grams of benzyl alcohol were added and the flask contents stirred at reflux for five hours to collect the water formed. A white substance precipitated from solution and was filtered. It was washed with hexane. The substance had a melting point of 96° C. to 98° C., a percent sulfur of 14.4 and a hydroxyl number of 259.

후처리

  1. temperatureat reflux for five hours
  2. customto collect the water
  3. customformed
  4. customA white substance precipitated from solution
  5. filtrationwas filtered
  6. washIt was washed with hexane

출처 및 근거

ORD 기록
ord-8075d74917aa444f98c7cce9ed6fb1d4
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04143076

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