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m-Chloroperbenzoic acid → 1-Acetyl-4-bromoindolin-3-one

HRID 1882219
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HRID 1882219 반응식
[C:1]([N:4]1[C:12]2[C:7](=[C:8]([Br:13])[CH:9]=[CH:10][CH:11]=2)[C:6](C=O)=[CH:5]1)(=[O:3])[CH3:2].ClC1C=CC=C(C(OO)=[O:24])C=1>C(Cl)Cl>[C:1]([N:4]1[C:12]2[C:7](=[C:8]([Br:13])[CH:9]=[CH:10][CH:11]=2)[C:6](=[O:24])[CH2:5]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 534157881-Acetyl-4-bromo-1H-indole-3-carbaldehyde

생성물 1

HCID 532432881-Acetyl-4-bromoindolin-3-one수율 26.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1-Acetyl-4-bromo-1H-indole-3-carbaldehyde (3.5 g, 13.2 mmol) was dissolved in CH2Cl2 (50 mL). 3-Chloroperbenzoic acid (3.9 g, 15.8 mmol) was added, and the reaction stirred 16 h at r.t. The solution was washed with sat. NaHCO3 and brine, dried (MgSO4), and concentrated. The residue was stirred with K2CO3 (100 mg) in MeOH (50 mL) for 2 min. The solution was concentrated and purified by silica gel chromatography (100% CH2Cl2) to give 880 mg (26%) of the title compound as a faintly blue solid. MS (ES) [m+H] calc'd for C10H8BrNO2, 254, 256; found 254, 256.

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후처리

  1. washThe solution was washed with sat. NaHCO3 and brine
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated
  4. stirringThe residue was stirred with K2CO3 (100 mg) in MeOH (50 mL) for 2 min
  5. concentrationThe solution was concentrated
  6. custompurified by silica gel chromatography (100% CH2Cl2)

출처 및 근거

ORD 기록
ord-a753f2890abc4f0ba6f7caa1d5869d7c
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318939B2

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