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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Azobisisobutyronitrile → Benzoic acid, 3-(bromomethyl)-4-fluoro-, methyl ester

HRID 1617210
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인쇄 미리보기

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HRID 1617210 반응식
C1C(=O)N([Br:8])C(=O)C1.CC(N=NC(C#N)(C)C)(C#N)C.[F:21][C:22]1[CH:31]=[CH:30][C:25]([C:26]([O:28][CH3:29])=[O:27])=[CH:24][C:23]=1[CH3:32]>CCOC(C)=O>[Br:8][CH2:32][C:23]1[CH:24]=[C:25]([CH:30]=[CH:31][C:22]=1[F:21])[C:26]([O:28][CH3:29])=[O:27]
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참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 18788764Methyl 4-fluoro-3-methylbenzoate

생성물 1

HCID 53419607Benzoic acid, 3-(bromomethyl)-4-fluoro-, methyl ester

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
80 °C

실험 절차

NBS (14.60 g) and AIBN (2.89 g) were added to a solution of the product from step (i) (9.85 g) in EtOAc (200 mL). The resulting mixture was stirred at 80° C. for 20 h. After cooling the mixture was washed with sat. sodium thiosulphate, brine, dried, filtered and the solvent removed. The crude product was purified using chromatography, to give the subtitle compound, 5.30 g.

후처리

  1. temperatureAfter cooling the mixture
  2. washwas washed with sat. sodium thiosulphate, brine
  3. customdried
  4. filtrationfiltered
  5. customthe solvent removed
  6. customThe crude product was purified

출처 및 근거

ORD 기록
ord-c5dd67bb22234be4aea0355aa8eafc20
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765939B2

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