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Aniline → (E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide

HRID 2061017
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반응식

HRID 2061017 반응식
[CH3:1]/[C:2](=[CH:6]\[S:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)/[C:3]([OH:5])=O.S(Cl)(Cl)=O.[NH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C1(C)C=CC=CC=1>[CH3:1]/[C:2](=[CH:6]\[S:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)/[C:3]([NH:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6115AnilineHCID 24386Thionyl ChlorideHCID 13152781(E)-2-methyl-3-(phenylthio)-2-propenoic acid

생성물 1

HCID 59498330(E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide수율 87%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A suspension of 2.5 g (12.8 mmol) of (E)-2-methyl-3-(phenylthio)-2-propenoic acid and 3.5 g (25.7 mmol) of thionyl chloride in 25 ml of toluene was refluxed for 1 hour and then concentrated under vacuum. The residue was dissolved in 25 ml of ethyl acetate and cooled in ice bath. To the solution was added dropwise 2.9 g (32 mmol) of aniline and stirred at room temperature for 30 minutes. The reaction mixture was washed sequentially with 1N HCl solution, a saturated NaHCO3 solution, and a saturated NaCl solution. The organic layer was dried over anhydrous MgSO4 and concentrated to obtain 3.0 g of (E)-2-Methyl-N-phenyl-3-(phenylthio)-2-propenamide.

후처리

  1. temperaturewas refluxed for 1 hour
  2. concentrationconcentrated under vacuum
  3. dissolutionThe residue was dissolved in 25 ml of ethyl acetate
  4. temperaturecooled in ice bath
  5. washThe reaction mixture was washed sequentially with 1N HCl solution
  6. dry with materialThe organic layer was dried over anhydrous MgSO4
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e063550b00564276b337739f6f0504d9
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278473B2

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