ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 536341
ノート
印刷プレビュー

反応式

HRID 536341 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-a209a1cc9d4e4e8f81abc95314bfd2ab
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859574B2

反応ノート

読み込み中…