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Water → 8-chloro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one

HRID 577474
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HRID 577474 반응식
[Cl:1][C:2]1[C:3]([O:13]C)=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10](=[O:12])[NH:9][CH2:8][CH2:7]2.B(Br)(Br)Br.O>C(Cl)Cl>[Cl:1][C:2]1[C:3]([OH:13])=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10](=[O:12])[NH:9][CH2:8][CH2:7]2
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참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 867237008-chloro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one

생성물 1

HCID 867237018-chloro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one수율 902.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a 0° C. solution of 8-chloro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (1d, 7.8 g, 3.7 mmol) in dry CH2Cl2 (120 mL) was added dropwise BBr3 (11 mL, 111 mmol). After the addition, the mixture was stirred at room temperature overnight. To the reaction mixture was added dropwise H2O (200 mL). The mixture was extracted with EtOAc (8×200 mL), dried over Na2SO4 and concentrated under vacuum. To the residue was added EtOAc (20 mL) and petroleum ether (40 mL). The mixture was filtered and the solids were dried under vacuum to give 8-chloro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one (1e, 6.6 g, 91%) as a brown solid.

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후처리

  1. additionAfter the addition
  2. extractionThe mixture was extracted with EtOAc (8×200 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under vacuum
  5. additionTo the residue was added EtOAc (20 mL) and petroleum ether (40 mL)
  6. filtrationThe mixture was filtered
  7. customthe solids were dried under vacuum

출처 및 근거

ORD 기록
ord-fc6a747341fd48dcb7ca9f40c780b479
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040515B2

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