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Phosphorus oxychloride → 1-Chloro-6-ethoxyisoquinoline

HRID 1895866
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HRID 1895866 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].O=P(Cl)(Cl)[Cl:17]>>[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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 POCl3 (4 mL) was heated at 110° C. for 3 h (clear solution obtained upon heating). After 3 h, the reaction mixture was concentrated under reduced pressure. The residue was poured into iced water (10 mL), pH was then adjusted to 10 with 3N NaOH and extracted with CHCl3 (3×25 mL). The combined CHCl3 layers were washed with brine and dried (MgSO4). The organic layer was then filtered and concentrated 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), pH
  4. extractionextracted with CHCl3 (3×25 mL)
  5. washThe combined CHCl3 layers were washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationThe organic layer was then filtered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4e2afd8362864769bffc312bc51ba35f
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08518874B2

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