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Boron tribromide → 3-Ethyl-3-(3-hydroxy-phenyl)-azepan-2-one

HRID 1594857
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반응식

HRID 1594857 반응식
B(Br)(Br)Br.[CH2:5]([C:7]1([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([O:21]C)[CH:16]=2)[CH2:13][CH2:12][CH2:11][CH2:10][NH:9][C:8]1=[O:14])[CH3:6]>C(Cl)Cl>[CH2:5]([C:7]1([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([OH:21])[CH:16]=2)[CH2:13][CH2:12][CH2:11][CH2:10][NH:9][C:8]1=[O:14])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 28154553-Ethyl-3-(3-methoxyphenyl)azepan-2-one

생성물 1

HCID 217062193-Ethyl-3-(3-hydroxy-phenyl)-azepan-2-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A 1M solution of BBr3 (7.1 mL, 7.1 mmol) in CH2Cl2 was added to 3-ethyl-3-(3-methoxy-phenyl)-azepan-2-one (as described in Step A above) (0.800 g, 0.323 mmol) dissolved in anhydrous CH2Cl2 (5 mL) at −78° C. After 48 h of stirring at room temperature, the reaction was quenched with H2O, extracted with CH2Cl2 (3×), dried (MgSO4), concentrated and purified using reverse phase chromatography (95/5-5/95 H2O/CH3CN with 0.1% TFA, flow=65 mL/min) to give the title compound.

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후처리

  1. customthe reaction was quenched with H2O
  2. extractionextracted with CH2Cl2 (3×)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. custompurified

출처 및 근거

ORD 기록
ord-493ef8c5f4894eeaa086fbd74133c8d7
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06284755B1

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