Potassium Carbonate → 1-Bromo-2-(2,4-difluorophenoxy)-4-methyl-5-nitrobenzene

HRID 1715608ノート

反応式

HRID 1715608 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5]([CH3:11])=[CH:4][C:3]=1Br.[F:13][C:14]1[CH:19]=[C:18]([F:20])[CH:17]=[CH:16][C:15]=1[OH:21].C([O-])([O-])=O.[K+].[K+]>>[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5]([CH3:11])=[CH:4][C:3]=1[O:21][C:15]1[CH:16]=[CH:17][C:18]([F:20])=[CH:19][C:14]=1[F:13]

参加物

4

反応物 3

HCID 11430Potassium CarbonateHCID 1230512,4-DifluorophenolHCID 574187581,2-Dibromo-4-methyl-5-nitrobenzene

生成物 1

HCID 574187591-Bromo-2-(2,4-difluorophenoxy)-4-methyl-5-nitrobenzene収率 95%

反応条件

温度
100 °C

実験手順

A mixture of 1,2-dibromo-4-methyl-5-nitrobenzene (84.3 g, 286 mmol), 2,4-difluorophenol (37.2 g, 286 mmol), and K2CO3 (43.5 g, 315 mmol) were heated to 100° C. for 45 hours. The reaction mixture was cooled to room temperature and then stored in a 5° C. refrigerator overnight. The reaction mixture was poured into 1200 mL of ice water all at once. The resulting damp solid was collected, partially ground up, and stirred in 900 mL H2O for 45 minutes. The solid was collected by filtration and rinsed with 700 mL of water portion-wise. The resulting solid was dried under high vacuum overnight to yield 93.5 g of a brown solid (95% yield). 1H NMR (400 mHz, CDCl3) δ 8.38 (s, 1H), 7.18 (m, 1H), 7.03 (m, 1H), 6.97 (m, 1H), 6.52 (s, 1H), 2.50 (s, 3H).

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customstored in a 5° C.
  3. customrefrigerator overnight
  4. customThe resulting damp solid was collected
  5. filtrationThe solid was collected by filtration
  6. washrinsed with 700 mL of water portion-wise
  7. customThe resulting solid was dried under high vacuum overnight

出典と根拠

ORDレコード
ord-a24a581791d24587a0f2769276975600
出典データセット
uspto-grants-2010_09
特許番号
US07799782B2

反応ノート

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