Water → 1-Methoxy-3-(methoxymethoxy)benzene

HRID 527538ノート

反応式

HRID 527538 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1.[H-].[Na+].[CH3:12][O:13][CH2:14]Br.O>O1CCCC1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH2:12][O:13][CH3:14])[CH:4]=1

参加物

6

実験手順

To a solution of 3-(methyloxy)phenol (10.38 g, 84 mmol) in tetrahydrofurane (100 ml, SCRC) was added NaH (60% wt., 1.824 g, 76 mmol, Aldrich) portionwise under ice-cooling. The reaction mixture was stirred at room temperature for 1 hour and bromomethyl methyl ether (9.5 g, 76 mmol, SCRC) was then added. The resulting mixture was stirred at room temperature for 2 hours and water (50 ml) was added. The reaction mixture was extracted with ethyl acetate (2 times 50 ml, SCRC) and the combined organic layers were dried over sodium sulphate, evaporated. The residue was purified by column chromatography on silica gel (EtOAc:PE=1:100) to afford the title compound (10.2 g) as a colorless liquid.

後処理

  1. temperaturecooling
  2. stirringThe resulting mixture was stirred at room temperature for 2 hours
  3. extractionThe reaction mixture was extracted with ethyl acetate (2 times 50 ml, SCRC)
  4. dry with materialthe combined organic layers were dried over sodium sulphate
  5. customevaporated
  6. customThe residue was purified by column chromatography on silica gel (EtOAc:PE=1:100)

出典と根拠

ORDレコード
ord-e4d4a27ef4de44df9930df7699d42182
出典データセット
uspto-grants-2016_05
特許番号
US09346790B2

反応ノート

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