Reaktion #1583834

ord-2e1fbe7e9df64bc880f247b6011844b0

Reaktionsgleichung

COC(=O)NCc1cc(I)ccc1Cl
methyl[(2-chloro-5-iodo-phenyl)methyl]carbamate
COC(=O)NCc1cc(I)ccc1Cl
product
COC(=O)NCc1cc(I)ccc1Cl
methyl[(2-chloro-5-iodo-phenyl)methyl]carbamate
C#C[Si](C)(C)C
ethynyltrimethylsilane
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
COC(=O)NCc1cc(C#C[Si](C)(C)C)ccc1Cl
title compound
COC(=O)NCc1cc(C#C[Si](C)(C)C)ccc1Cl
methyl N-[[2-chloro-5-[2-(trimethylsilyl)ethynyl]-phenyl]methyl]carbamate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated onto silica gel (7 g)
  2. 2
    Sonstigepurified by medium pressure liquid chromatography (0 to 25% gradient of ethyl acetate in hexanes as eluant)

Vorschrift

A mixture methyl[(2-chloro-5-iodo-phenyl)methyl]carbamate (i.e. the product of Step B) (3.0 g, 9.2 mmol), ethynyltrimethylsilane (1.94 mL, 13.8 mmol), bis(triphenylphosphine)palladium(II) dichloride (0.032 g, 0.05 mmol), copper(I) iodide (0.018 g, 0.09 mmol), triphenylphosphine (0.024 g, 0.09 mmol) in tetrahydrofuran (18 mL) and triethylamine (18 mL) was stirred at room temperature for 30 minutes. The reaction mixture was concentrated onto silica gel (7 g) and then purified by medium pressure liquid chromatography (0 to 25% gradient of ethyl acetate in hexanes as eluant) to provide the title compound as an oil (1.37 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198433B2uspto-grants-2015_12