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Potassium Carbonate → 2-Bromo-1-methoxy-4-(2-methoxy-ethoxy)-benzene

HRID 1469373
ノート
印刷プレビュー

反応式

HRID 1469373 の反応式
[CH3:1][O:2][CH2:3][CH2:4]Br.C(=O)([O-])[O-].[K+].[K+].[Br:12][C:13]1[CH:14]=[C:15]([OH:21])[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]>CN(C=O)C>[Br:12][C:13]1[CH:14]=[C:15]([O:21][CH2:4][CH2:3][O:2][CH3:1])[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]
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

5

反応物 3

HCID 11430Potassium CarbonateHCID 809722-Bromoethyl methyl etherHCID 6088153-Bromo-4-methoxyphenol

生成物 1

HCID 580730982-Bromo-1-methoxy-4-(2-methoxy-ethoxy)-benzene収率 88.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

2-bromoethyl methyl ether (0.07 mL, 0.74 mmol) was added to a mixture of potassium carbonate (136 mg, 0.99 mmol) and 3-bromo-4-methoxy-phenol (100 mg, 0.49 mmol) in DMF (2 mL) and mix heated at 100° C. for 1 hr. Reaction mixture was allowed to cool and partitioned between ethyl acetate (20 mL×2) and water (20 mL). The combined organic phases were washed with sat. aqueous sodium chloride solution (40 mL) and dried over sodium sulphate. Solvents were removed in vacuo to afford a crude oil which was purified by flash chromatography on silica gel, eluting with a gradient of 0-10% ethyl acetate in hexane to afford the title compound (113 mg, 88%) as a colourless liquid.

後処理

  1. additionmix
  2. customReaction mixture
  3. temperatureto cool
  4. custompartitioned between ethyl acetate (20 mL×2) and water (20 mL)
  5. washThe combined organic phases were washed with sat. aqueous sodium chloride solution (40 mL)
  6. dry with materialdried over sodium sulphate
  7. customSolvents were removed in vacuo
  8. customto afford a crude oil which
  9. customwas purified by flash chromatography on silica gel
  10. washeluting with a gradient of 0-10% ethyl acetate in hexane

出典と根拠

ORDレコード
ord-c9c16d86b369446e9ac1e86a9cf24007
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09006269B2

反応ノート

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