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Isopropanol → 1-Bromo-5-isopropoxy-2-methyl-4-nitrobenzene

HRID 1897662
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인쇄 미리보기

반응식

HRID 1897662 반응식
[Br:1][C:2]1[CH:7]=[C:6](F)[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[CH3:12].C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:19][CH:20]([OH:22])[CH3:21]>>[Br:1][C:2]1[CH:7]=[C:6]([O:22][CH:20]([CH3:21])[CH3:19])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[CH3:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 3776IsopropanolHCID 10796Cesium carbonateHCID 534032861-Bromo-5-fluoro-2-methyl-4-nitrobenzene

생성물 1

HCID 671555871-Bromo-5-isopropoxy-2-methyl-4-nitrobenzene

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온도
50 °C

실험 절차

To a solution of 1-bromo-5-fluoro-2-methyl-4-nitrobenzene (Step 1, 1.5 g, 6.4 mmol) in 2-propanol (30 mL) was added cesium carbonate (5.3 g, 16 mmol). The mixture was heated at 50° C. overnight. The mixture was concentrated and partitioned between ethyl acetate and water. The organic layer was concentrated and the residue was purified with silica gel column chromatography with 5% ethyl acetate in hexanes to afford 1-bromo-5-isopropoxy-2-methyl-4-nitrobenzene as a yellow solid.

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후처리

  1. concentrationThe mixture was concentrated
  2. custompartitioned between ethyl acetate and water
  3. concentrationThe organic layer was concentrated
  4. customthe residue was purified with silica gel column chromatography with 5% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-5eb66d1a3a484a2ca7d2dce9bc4c5cfd
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519129B2

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