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Sodium Hydroxide → (2E)-N-[3-(Trifluoromethyl)phenyl]-2H-quinolizin-2-imine

HRID 1973387
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반응식

HRID 1973387 반응식
[Br-].[F:2][C:3]([F:22])([F:21])[C:4]1[CH:5]=[C:6]([CH:18]=[CH:19][CH:20]=1)[NH:7][C:8]1[CH:17]=[CH:16][N+:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1.[OH-].[Na+]>O>[F:22][C:3]([F:2])([F:21])[C:4]1[CH:5]=[C:6]([N:7]=[C:8]2[CH:17]=[CH:16][N:15]3[C:10]([CH:11]=[CH:12][CH:13]=[CH:14]3)=[CH:9]2)[CH:18]=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 124465292-[3-(Trifluoromethyl)anilino]quinolizin-5-ium bromide

생성물 1

HCID 330199(2E)-N-[3-(Trifluoromethyl)phenyl]-2H-quinolizin-2-imine

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a suspension of 2-(3-trifluoromethylanilino)quinolizinium bromide (22 g., 0.060 mole) in H2O (400 ml) was added a solution of NaOH (25 g., 0.62 mole) in H2O (250 ml). The mixture was stirred at about 50° for 1 hour, then chilled and filtered. The yellow product weighed 17 g (97%). The sample was boiled in benzene, filtered and diluted with hexane. Evaporation of the solvent gave yellow crystals which melted at 134°-135°.

후처리

  1. temperaturechilled
  2. filtrationfiltered
  3. filtrationfiltered
  4. additiondiluted with hexane
  5. customEvaporation of the solvent
  6. customgave yellow crystals which melted at 134°-135°

출처 및 근거

ORD 기록
ord-8f9fc8fbaeb2447bafef26e5adac6538
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03997547

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