Reaktion #8219

ord-4866853a2f2646d1ab550d48cec29d92

Reaktionsgleichung

COC(=O)c1cccc2[nH]cc(CN(C)C)c12.I
3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide
COS(=O)(=O)OC
dimethyl sulfate
C[O-].[Na+]
sodium methoxide
CC(C)[N+](=O)[O-]
2-nitropropane
COC(=O)c1cccc2[nH]cc(CC(C)(C)[N+](=O)[O-])c12
3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe aqueous layer is extracted with ethyl acetate (200 ml)
  2. 2
    Trocknenthe combined organic layers are dried over Na2SO4
  3. 3
    Einengenconcentrated in vacuo

Vorschrift

A 0° C. solution of 3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide (19 g, 52.7 mmol) in 75 ml of methanol and 75 ml of 2-nitropropane is treated with dimethyl sulfate (10 ml, 105.5 mmol) and solid sodium methoxide (6.3 g, 110.6.mmol) sequentially. The resulting mixture is allowed to warm to ambient temperature, and, after stirring overnight, the reaction mixture is diluted with ethyl acetate (300 ml) and saturated aqueous NH4Cl solution (500 ml). The aqueous layer is extracted with ethyl acetate (200 ml), and the combined organic layers are dried over Na2SO4 and concentrated in vacuo to give 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester in quantitative yield.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087635B2uspto-grants-2006_08