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Diethyl Ether → 8-Methoxy-1,2,3,4-tetrahydro-9-acridinamine

HRID 981919
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인쇄 미리보기

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HRID 981919 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([NH2:11])[C:8]=1[C:9]#[N:10].CCO[CH2:15][CH3:16]>[N+](C1C=CC=CC=1)([O-])=O.C1(=O)CCCCC1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:8]=1[C:9]([NH2:10])=[C:15]1[C:16]([CH2:4][CH2:3][CH2:8][CH2:7]1)=[N:11]2
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참가 물질

5

반응물 2

HCID 3283Diethyl EtherHCID 127157142-Amino-6-methoxybenzonitrile

생성물 1

HCID 197702928-Methoxy-1,2,3,4-tetrahydro-9-acridinamine

시약·촉매·용매 2

HCID 7416Nitrobenzene용매HCID 7967Cyclohexanone용매

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온도
125 °C

실험 절차

6-Methoxyanthranilonitrile (14.0 g) was dissolved in nitrobenzene (150 ml) and cyclohexanone (18.45 g), and freshly fused zinc chloride (25.6 g) was added. The reaction mixture was warmed at 125° C. for 1.5 hr, cooled to room temperature, and poured into ether (1 l). The solid was collected, washed with ether, and distributed between 2-butanone and ammonium hydroxide. The organic phase was washed with brine, dried, filtered, and evaporated. The residue was recrystallized two times from ethyl acetate to give 13.7 g (63.8%), mp 187°-188° C.

후처리

  1. temperaturecooled to room temperature
  2. customThe solid was collected
  3. washwashed with ether
  4. washThe organic phase was washed with brine
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was recrystallized two times from ethyl acetate
  9. customto give 13.7 g (63.8%), mp 187°-188° C.

출처 및 근거

ORD 기록
ord-743d82cf4e014a36a800348797365806
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04994452

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