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

HRID 1897662
ノート
印刷プレビュー

反応式

HRID 1897662 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

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

生成物 1

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

反応条件

温度
50 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-5eb66d1a3a484a2ca7d2dce9bc4c5cfd
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08519129B2

反応ノート

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