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Potassium Carbonate → N-but-3-en-1-yl-N-(4-methoxyphenyl)acrylamide

HRID 564383
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HRID 564383 반응식
[CH2:1]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][CH:7]=1)[CH2:2][CH:3]=[CH2:4].C([O-])([O-])=O.[K+].[K+].[C:20](Cl)(=[O:23])[CH:21]=[CH2:22]>C(Cl)Cl>[CH2:1]([N:5]([C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[CH:10][CH:11]=1)[C:20](=[O:23])[CH:21]=[CH2:22])[CH2:2][CH:3]=[CH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 13140Acryloyl chlorideHCID 44131193N-but-3-en-1-yl-4-methoxyaniline

생성물 1

HCID 67004663N-but-3-en-1-yl-N-(4-methoxyphenyl)acrylamide수율 89%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of N-but-3-en-1-yl-4-methoxyaniline (340 mg, 1.92 mmol) in methylene chloride (5 mL) was added K2CO3 (530 mg, 3.80 mmol) and acryloyl chloride (234 μL, 2.88 mmol) at 0° C. After 15 min., the reaction was quenched with NaHCO3 (2 mL, sat. aq.) and the organic layer was isolated, concentrated and subjected to flash chromatography (Hexanes:EtOAc 4:1) to yield N-but-3-en-1-yl-N-(4-methoxyphenyl)acrylamide (395 mg, 89%).

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후처리

  1. customthe reaction was quenched with NaHCO3 (2 mL, sat. aq.)
  2. customthe organic layer was isolated
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8acc044da1214e2d9d48fc7f8e5af148
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08067457B2

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