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2-Methoxyethanol → 2-Fluoro-1-(2-methoxyethoxy)-4-nitrobenzene

HRID 1842871
ノート
印刷プレビュー

反応式

HRID 1842871 の反応式
[CH3:1][O:2][CH2:3][CH2:4][OH:5].C([O-])([O-])=O.[K+].[K+].F[C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][C:14]=1[F:22]>CN(C=O)C.O>[F:22][C:14]1[CH:15]=[C:16]([N+:19]([O-:21])=[O:20])[CH:17]=[CH:18][C:13]=1[O:5][CH2:4][CH2:3][O:2][CH3:1]
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

6

反応物 3

HCID 80192-MethoxyethanolHCID 11430Potassium CarbonateHCID 1230531,2-Difluoro-4-nitrobenzene

生成物 1

HCID 234980752-Fluoro-1-(2-methoxyethoxy)-4-nitrobenzene収率 74%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

反応条件

温度
70 °C

実験手順

To a stirred suspension of methyl glycol (2.2 mL, 28.28 mmol, 1.5 eq.) and K2CO3 (7.8 g, 56.60 mmol, 3.0 eq.) in DMF (20 mL) was added 1,2-difluoro-4-nitrobenzene (3.0 g, 18.85 mmol, 1.0 eq.) and the mixture was stirred for 16 h at 70° C. The reaction mixture was cooled and diluted with water (30 mL) and extracted with ethyl acetate (40 mL). The organic layer was separated and washed with water (50 mL), brine (50 mL), and dried over sodium sulfate and the solvent evaporated under vacuum. The crude product was washed with n-pentane (30 mL) to obtain 2-fluoro-1-(2-methoxyethoxy)-4-nitrobenzene (3 g, 74%, as solid; TLC system: EtOAc/PE (1:9), Rf: 0.2).

後処理

  1. temperatureThe reaction mixture was cooled
  2. extractionextracted with ethyl acetate (40 mL)
  3. customThe organic layer was separated
  4. washwashed with water (50 mL), brine (50 mL)
  5. dry with materialdried over sodium sulfate
  6. customthe solvent evaporated under vacuum
  7. washThe crude product was washed with n-pentane (30 mL)

出典と根拠

ORDレコード
ord-d5a4234134e841448a6f4a36a82ac52f
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946204B2

反応ノート

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