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Phosphorus oxychloride → 4-Chloro-7-methylquinoline-2-carbonitrile

HRID 922749
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HRID 922749 반응식
[CH3:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]#[N+:13][O-])=[N:9]2)=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:17]>C(Cl)(Cl)Cl>[Cl:17][C:6]1[C:5]2[C:10](=[CH:11][C:2]([CH3:1])=[CH:3][CH:4]=2)[N:9]=[C:8]([C:12]#[N:13])[CH:7]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 895438927-methylquinoline-2-carbonitrile N-oxide

생성물 1

HCID 597749194-Chloro-7-methylquinoline-2-carbonitrile

시약·촉매·용매 1

HCID 6212Chloroform용매

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온도
70 °C

실험 절차

7-Methylquinoline-2-carbonitrile N-oxide (1-4, 5.3 g, 28.8 mmol, 1.0 equiv.) was dissolved in CHCl3 (80 ml, 0.36 M), and POCl3 was added (16.09 ml, 173 mmol, 6.0 equiv.). The mixture was heated to 70° C. overnight, quenched onto crushed ice and extracted three times with dichloromethane. The combined organic layers were washed with water followed by saturated aqueous sodium bicarbonate, dried over MgSO4, filtered and the solvent was removed to yield crude yellow solid. Recrystallization from heptane/EtOAc gave 95 g of 4-chloro-7-methylquinoline-2-carbonitrile (1-5). LRMS m/z (M+H)+203.2 found, 203.6 required.

후처리

  1. customquenched
  2. customonto crushed ice
  3. extractionextracted three times with dichloromethane
  4. washThe combined organic layers were washed with water
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customthe solvent was removed
  8. customto yield crude yellow solid
  9. customRecrystallization from heptane/EtOAc

출처 및 근거

ORD 기록
ord-df894fe17f194b8fba3d14d621e8d34e
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278960B2

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