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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(NE)-N-[(5-bromo-2-fluoro-3-methylphenyl)methylidene]hydroxylamine → 5-Bromo-2-fluoro-3-methyl-benzonitrile

HRID 1503040
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인쇄 미리보기

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HRID 1503040 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH3:12])[C:5]([F:11])=[C:6]([CH:10]=1)/[CH:7]=[N:8]/O>C(OC(=O)C)(=O)C.O>[Br:1][C:2]1[CH:3]=[C:4]([CH3:12])[C:5]([F:11])=[C:6]([CH:10]=1)[C:7]#[N:8]
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참가 물질

4

반응물 1

HCID 89306402(NE)-N-[(5-bromo-2-fluoro-3-methylphenyl)methylidene]hydroxylamine

생성물 1

HCID 711383595-Bromo-2-fluoro-3-methyl-benzonitrile

시약·촉매·용매 2

HCID 962Water용매HCID 7918Acetic Anhydride용매

실험 절차

A stirred solution of (E)-5-bromo-2-fluoro-3-methylbenzaldehyde oxime (0.5 g, 2.2 mmol) in acetic anhydride (5.0 mL) was heated to reflux for 18 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined ethyl acetate layer was washed with brine and dried over Na2SO4 and concentrated under reduced pressure to afford the crude compound as a light brown gummy material (0.4 g, crude): ESIMS m/z 213.82 ([M+H]+).

후처리

  1. temperatureto reflux for 18 h
  2. extractionextracted with ethyl acetate
  3. washThe combined ethyl acetate layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-87efe7e498914b599e71f32e2a83f8e8
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09211281B2

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