反応 #486419

ord-ca06278ce1d2408d931bcac9251c13b0

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwere dropwise added
  2. 2
    その他it was then quenched cautiously by the addition of cold dilute HCl
  3. 3
    抽出extracted with EtOAc
  4. 4
    抽出The EtOAc extract
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    洗浄was washed successively with
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    その他After drying
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    ろ過(MgSO4) filtration and evaporation
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    その他gave liquid
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    workup.DISTILLATIONThe product was purified by distillation (85° C., 0.2 mm Hg)

実験手順

To a suspension of NaH (2.5 g, 0.06 mol) in dry DMF (100 mL) at 0° C. was added solution of 1-bromo-2-hydroxy-4-methoxybenzene (10.6 g, 0.05 mol). After stirring at 0° C. for 30 min. bromomethyl methyl ether (7.8 g, 0.06 mmol) were dropwise added. The mixture was warmed to room temperature over 20 min. and then stirred for 2 h, it was then quenched cautiously by the addition of cold dilute HCl and extracted with EtOAc. The EtOAc extract was washed successively with; H2O, 5% aqueous NaHCO3, H2O and finally brine. After drying (MgSO4) filtration and evaporation gave liquid. The product was purified by distillation (85° C., 0.2 mm Hg) to give the title compound as a colorless oil (13.7 g, 97%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05817693uspto-grants-1998_10