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Phosphorus oxychloride → 1-Chloro-6-ethoxyisoquinoline

HRID 1511466
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HRID 1511466 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[C:10](=O)[NH:9][CH:8]=[CH:7]2)[CH3:2].P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:10]1[C:11]2[C:6](=[CH:5][C:4]([O:3][CH2:1][CH3:2])=[CH:13][CH:12]=2)[CH:7]=[CH:8][N:9]=1
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 578930896-Ethoxyisoquinolin-1(2H)-one

생성물 1

HCID 578931101-Chloro-6-ethoxyisoquinoline수율 88%

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온도
110 °C

실험 절차

A suspension of 6-ethoxy-2H-isoquinolin-1-one (896 mg, 4.74 mmol) in phosphorus oxychloride (POCl3, 4 mL) was heated at 110° C. for 3 hours (clear solution obtained upon heating). After 3 hours, the reaction mixture was concentrated under reduced pressure. The residue was poured into iced water (10 mL), the pH adjusted to 10 with 3N sodium hydroxide, and the mixture extracted with chloroform (3×25 mL). The combined chloroform layers were washed with brine and dried over magnesium sulfate. The organic layer was then filtered and concentrated under reduced pressure to give 1-chloro-6-ethoxy-isoquinoline (866 mg, 4.18 mmol, 88% yield, >90% pure) as tan solid. MS m/z 208 (M++H).

후처리

  1. custom(clear solution obtained upon heating)
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. additionThe residue was poured into iced water (10 mL)
  4. extractionthe mixture extracted with chloroform (3×25 mL)
  5. washThe combined chloroform layers were washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationThe organic layer was then filtered
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-37e211e471ad46f1ac661e27fb972608
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211897B2

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