1-Bromo-2-Chloroethane → HCID 22326897、化合物

HRID 601032ノート

反応式

HRID 601032 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:4]=1[OH:12].Br[CH2:14][CH2:15][Cl:16].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Cl:16][CH2:15][CH2:14][O:12][C:4]1[CH:5]=[CH:6][C:7]([N+:9]([O-:11])=[O:10])=[CH:8][C:3]=1[O:2][CH3:1]

参加物

5

反応条件

温度
90 °C

実験手順

A mixture of 2-methoxy-4-nitro-phenol (2.50 g, 14.8 mmol), 1-bromo-2-chloro-ethane (1.35 mL, 16.3 mmol) and potassium carbonate (4.08 g, 29.6 mmol) in DMF (50 mL) in a sealed tube was heated at 90° C. for 18 h. The reaction was cooled and filtered, washing with ethyl acetate. The filtrate was washed with sodium bicarbonate, water (4 times) and brine, was dried (sodium sulfate) and evaporated. Purification by flash chromatography (SiO2) eluted with 35:65 ethyl acetate:hexanes provided 1-(2-chloro-ethoxy)-2-methoxy-4-nitro-benzene (1.93 g, 56% yield) as an off-white solid. 1H-NMR (DMSO-d6, 500 MHz) 7.89 (dd, 1H), 7.76 (d, 1H), 7.21 (d, 1H), 4.41 (t, 2H), 4.00 (t, 2H), 3.90 (s, 3H) ppm; HPLC (Method A) 3.781 min.

後処理

  1. temperatureThe reaction was cooled
  2. filtrationfiltered
  3. washwashing with ethyl acetate
  4. washThe filtrate was washed with sodium bicarbonate, water (4 times) and brine
  5. dry with materialwas dried (sodium sulfate)
  6. customevaporated
  7. customPurification by flash chromatography (SiO2)
  8. washeluted with 35:65 ethyl acetate

出典と根拠

ORDレコード
ord-86fe6a3a92ec425d8b5f686d0b34f3d5
出典データセット
uspto-grants-2011_03
特許番号
US07902239B2

反応ノート

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