Reaktion #69518

ord-02496be81bb3406ea0711670738f8315

Reaktionsgleichung

CC(C)CCON=O
isoamyl nitrite
CCOC(=O)c1cc(Cl)c(N)c(OC)c1
ethyl 4-amino-3-chloro-5-methoxybenzoate
CC#N
acetonitrile
ICI
diiodomethane
CCOC(=O)c1cc(Cl)c(I)c(OC)c1
title compound
Ausbeute 66.6%
CCOC(=O)c1cc(Cl)c(I)c(OC)c1
Ethyl 3-chloro-4-iodo-5-methoxybenzoate
Ausbeute 66.6%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe mixture was stirred at 70° C. for 40 minutes
  2. 2
    Sonstigewas returned to room temperature
  3. 3
    workup.DISTILLATIONthe solvent was then distilled off under reduced pressure
  4. 4
    Sonstigethe residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate

Vorschrift

To ethyl 4-amino-3-chloro-5-methoxybenzoate (15.8 g, 68.8 mmol), were added acetonitrile (40 mL) and diiodomethane (22.2 mL, 275 mmol) in this order, and the mixture was stirred at 70° C., and then isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise thereto over 10 minutes. The mixture was stirred at 70° C. for 40 minutes. The mixture was returned to room temperature, the solvent was then distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=8/1 then 5/1) to obtain the title compound (15.6 g, 45.8 mmol)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530504B2uspto-grants-2013_09