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Ammonium Chloride → 7-Bromo-5-fluoroquinoline

HRID 1621838
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HRID 1621838 반응식
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[C:5](/[CH:11]=[CH:12]/[CH:13]=O)=[C:4]([F:15])[CH:3]=1.[Cl-].[NH4+]>C(O)C.[Fe]>[Br:1][C:2]1[CH:7]=[C:6]2[C:5]([CH:11]=[CH:12][CH:13]=[N:8]2)=[C:4]([F:15])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 25517Ammonium ChlorideHCID 86647069(E)-3-(4-bromo-2-fluoro-6-nitrophenyl)acrylaldehyde

생성물 1

HCID 666003857-Bromo-5-fluoroquinoline수율 55.5%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

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온도
120 °C

실험 절차

A glass microwave reaction vessel was charged with (E)-3-(4-bromo-2-fluoro-6-nitrophenyl)acrylaldehyde (35 mg, 0.128 mmol), iron powder (0.018 mL, 2.55 mmol, Aldrich) and ammonium chloride (6.83 mg, 0.128 mmol, Aldrich) in ethanol (1 mL). The reaction mixture was stirred and heated in an Emrys Optimizer microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 120° C. for 5 min. The mixture was filtered through a pad of Celite® (diatomaceous earth), washed with EtOAc. The solvent was removed in vacuo and the residue was purified by silica gel chromatography eluting with 20% EtOAc/hexanes to give 7-bromo-5-fluoroquinoline (16 mg, 0.071 mmol, 55.4% yield). 1H NMR (300 MHz, CDCl3) δ 7.20-7.34 (m, 1H) 7.59-7.74 (m, 1H) 7.90 (d, J=8.48 Hz, 1H) 8.58 (d, J=1.61 Hz, 1H) 8.95 (d, J=2.34 Hz, 1H). m/z (ESI, +ve ion) 227.9 (M+H)+.

후처리

  1. customA glass microwave reaction vessel
  2. filtrationThe mixture was filtered through a pad of Celite® (diatomaceous earth)
  3. washwashed with EtOAc
  4. customThe solvent was removed in vacuo
  5. customthe residue was purified by silica gel chromatography
  6. washeluting with 20% EtOAc/hexanes

출처 및 근거

ORD 기록
ord-dde9d5f7e0ed4d3abb2c7dd9ce3a7ac1
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772480B2

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