Réaction #1583834

ord-2e1fbe7e9df64bc880f247b6011844b0

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09198433B2uspto-grants-2015_12