反応 #6468

ord-8e62ba77ab194d9c9cc5595ca51f8d17

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted 2×500 ml ethyl acetate
  2. 2
    洗浄washed 2×500 ml H2O and 1×300 ml brine
  3. 3
    乾燥dried (Na2SO4)
  4. 4
    その他chromatographed on silica gel using 1:1 hexane

実験手順

To 5-benzyloxy-2-methoxyphenacyl bromide (4.0 g, 0.0119 mol) in 80 ml of dry dimethylformamide was added 3-hydroxypyridine (1.24 g, 0.013 mol, 1.1 equiv) followed by NaH (50% in oil, 0.604 g, 1.1 equiv). After stirring for 18 hours under N2, the mixture was poured into 500 ml of ice and water, and extracted 2×500 ml ethyl acetate. The organic layers were combined, washed 2×500 ml H2O and 1×300 ml brine, dried (Na2SO4), stripped to an oil, and chromatographed on silica gel using 1:1 hexane:ethyl acetate as eluant to yield 1.07 g of present title product as a solid; IR(KBr) 1670 cm-1;MS 349 (M+); 1H-NMR (300 MHz, CDCl3) delta (ppm) 3.95 (s, 3H), 5.1 (s, 2H), 5.35 (s, 2H), 2.0 (d, 1 H), 7.2-7.5 (m, 8H), 7.6 (d, 1H), 8.3 (d, 1H), 8.4 (d, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05248685uspto-grants-1993_09