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5-Bromo-6-methoxy-2-methylquinoline → 475682-40-7

HRID 859996
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인쇄 미리보기

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HRID 859996 반응식
[Br:1][C:2]1[C:11]([O:12]C)=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH3:14])=[N:7]2>Br>[BrH:1].[Br:1][C:2]1[C:11]([OH:12])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH3:14])=[N:7]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 114252565-Bromo-6-methoxy-2-methylquinoline

생성물 1

HCID 86593645475682-40-7수율 182.3%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
5 °C

실험 절차

A mixture of 5-bromo-2-methyl-6-methoxyquinoline (30 g, 0.12 mol) in 48% HBr (135 mL) was heated to reflux for 7 hours then cooled to 5° C. in 1 hour to give a brown and thick slurry. The slurry was stirred at 0–5° C. for 1 hour then filtered, washed with EtOAc (2×50 mL) and dried in a vacuum oven to give 34.9 g (92%) of the title compound as a brown solid: 1H NMR (DMSO) δ 8.26 (d, J=8.7 Hz, 1H), 7.85 (d, J=9.1 Hz, 1H), 7.56 (d, J=9.1 Hz, 1H), 7.45 (d, J=8.7 Hz, 1H), 2.64 (s, 3H); 13C NMR (DMSO) δ 155.7, 152.0, 142.8, 133.3, 128.9, 126.4, 123.3, 121.2, 103.3, 24.1.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 7 hours
  3. customto give a brown and thick slurry
  4. filtrationthen filtered
  5. washwashed with EtOAc (2×50 mL)
  6. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-14027bfabecb4648b4ba48efb6a5533b
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07153849B2

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