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Acrylamide → 3-[{2-(1,3-Benzodioxol-5-yl)ethyl}thio]propionamide

HRID 486904
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HRID 486904 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][SH:12])=[CH:9][C:4]=2[O:3][CH2:2]1.[C:13]([NH2:17])(=[O:16])[CH:14]=[CH2:15]>C(O)C>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][S:12][CH2:15][CH2:14][C:13]([NH2:17])=[O:16])=[CH:9][C:4]=2[O:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6579AcrylamideHCID 158195122-(1,3-Benzodioxol-5-yl)ethanethiol

생성물 1

HCID 190016823-[{2-(1,3-Benzodioxol-5-yl)ethyl}thio]propionamide수율 60.4%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

5 g of 2-(1,3-benzodioxol-5-yl)ethanethiol and 4 g of acrylamide were dissolved in 100 ml of ethanol and the solution was heated under reflux to conduct the reaction for 20 h. The reaction mixture was cooled with ice. 100 ml of ethanol was added thereto and crystals thus formed were recovered by filtration to obtain 4.2 g of the intended compound in the form of colorless needles.

후처리

  1. temperaturethe solution was heated
  2. temperatureunder reflux
  3. customthe reaction for 20 h
  4. temperatureThe reaction mixture was cooled with ice
  5. customcrystals thus formed
  6. filtrationwere recovered by filtration

출처 및 근거

ORD 기록
ord-484311cae6004b7e98f916784b017118
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05292901

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