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N-bromobutanimide → Methyl 3-amino-6-bromo-5-fluoro-2-methylbenzoate

HRID 887780
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HRID 887780 반응식
[NH2:1][C:2]1[C:3]([CH3:13])=[C:4]([CH:9]=[C:10]([F:12])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[Br:14]N1C(=O)CCC1=O>C(#N)C>[NH2:1][C:2]1[C:3]([CH3:13])=[C:4]([C:9]([Br:14])=[C:10]([F:12])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 53419617Methyl 3-amino-5-fluoro-2-methylbenzoate

생성물 1

HCID 59145869Methyl 3-amino-6-bromo-5-fluoro-2-methylbenzoate수율 89.7%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of methyl 3-amino-5-fluoro-2-methylbenzoate (1.37 g, 7.48 mmol) in acetonitrile (57 mL) was added N-bromosuccinimide (1.01 g, 5.66 mmol) under ice-cooling, and the mixture was stirred for 2 hr. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→30/70) to give the title compound (1.33 g, yield 68%).

후처리

  1. temperaturecooling
  2. concentrationThe reaction solution was concentrated under reduced pressure
  3. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→30/70)

출처 및 근거

ORD 기록
ord-dcc2122e14cb48eb99102b147426f582
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08247429B2

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