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Methylamine → 3-{4-[(3-Fluorophenyl)methoxy]phenyl}-N-methylprop-2-enamide

HRID 2184360
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HRID 2184360 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][CH:20]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]=[CH:14][C:15](Cl)=[O:16])=[CH:9][CH:8]=1.[CH3:21][NH2:22]>ClCCl.O>[F:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][CH:20]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]=[CH:14][C:15]([NH:22][CH3:21])=[O:16])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6329MethylamineHCID 713776793-{4-[(3-Fluorophenyl)methoxy]phenyl}prop-2-enoyl chloride

생성물 1

HCID 686684993-{4-[(3-Fluorophenyl)methoxy]phenyl}-N-methylprop-2-enamide수율 30%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

500 mg (1.72 mmol) of the crude 3-[4-(3-fluoro-benzyloxy)-phenyl]-acryloyl chloride is dissolved in 2 ml dichloromethane and 0.4 ml of a 41% solution of methylamine in water is added. The reaction mixture is heated under reflux for about 3 hours, cooled, filtered and washed with cold dichloromethane to yield 149 mg (30%) of a colorless solid. MS: m/e=286.2 (M+).

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후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for about 3 hours
  3. temperaturecooled
  4. filtrationfiltered
  5. washwashed with cold dichloromethane

출처 및 근거

ORD 기록
ord-1f439d76a4bb4fbb8bfe9418063e8ebc
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06900354B2

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