反応 #2047417

ord-e3ca3b84aa9141468770732f453bc391

反応方程式

O
Water
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2[nH]1
ethyl 7-nitro-1H-indole-2-carboxylate
[H-].[Na+]
sodium hydride
COCCl
Chloromethyl methyl ether
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
title compound
収率 77.0%
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
ethyl 1-(methoxymethyl)-7-nitro -1H-indole-2-carboxylate
収率 77.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他at 0° C.
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hr
  3. 3
    抽出the mixture was extracted with ethyl acetate
  4. 4
    洗浄The ethyl acetate layer was washed with saturated brine
  5. 5
    乾燥dried (MgSO4)
  6. 6
    濃縮concentrated

実験手順

To a suspension of sodium hydride (60%, in oil, 0.51 g) in N,N-dimethylformamide (15 ml) was slowly added ethyl 7-nitro-1H-indole-2-carboxylate (2.50 g) at 0° C., and the mixture was stirred for 30 min. Chloromethyl methyl ether (1.00 ml) was added to the reaction mixture over 20 min at 0° C., and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (2.29 g, yield 77%) as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio). melting point 62-63° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08410087B2uspto-grants-2013_04