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3-Methoxybenzenethiol → HCID 10969180, 화합물

HRID 1859309
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인쇄 미리보기

반응식

HRID 1859309 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([SH:9])[CH:6]=[CH:7][CH:8]=1.[CH3:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([C:18](=[CH2:22])[C:19]([OH:21])=[O:20])=[CH:14][CH:13]=1>>[CH3:10][O:11][C:12]1[CH:13]=[CH:14][C:15]([CH:18]([CH2:22][S:9][C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[CH:4]=2)[C:19]([OH:21])=[O:20])=[CH:16][CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 849893-MethoxybenzenethiolHCID 145737872-(4-Methoxyphenyl)prop-2-enoic acid

생성물 1

HCID 10969180HCID 10969180, 화합물

반응 조건

온도
125 °C

실험 절차

3-Methoxybenzenethiol(2.5 ml, 20.1 mmol) was added to 2-(4-methoxyphenyl)acrylic acid (3 g, 16.8 mmol) and stirred for 21 hours with heating at 125° C. The reaction solution was extracted with diethyl ether, and the ether solution was washed with 0.1N iodine-potassium iodide solution, water and saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The residue was concentrated under reduced pressure to remove the organic solvent to obtain the title compound as a brown oil. The resulting compound was used in the next reaction without further purification.

후처리

  1. extractionThe reaction solution was extracted with diethyl ether
  • washthe ether solution was washed with 0.1N iodine-potassium iodide solution, water and saturated sodium chloride solution
  • dry with materialdried over anhydrous magnesium sulfate
  • concentrationThe residue was concentrated under reduced pressure
  • customto remove the organic solvent
  • 출처 및 근거

    ORD 기록
    ord-a10e9896b75e495b8ddaf9a951b99895
    출처 데이터셋
    uspto-grants-2000_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06153768

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