Réaction #684952

ord-7663ec31b19a44d0b3295f79ec346672

Équation de réaction

O=C([O-])O.[Na+]
sodium hydrogencarbonate
CS(=O)(=O)Cl
Methanesulfonyl chloride
CCN(CC)CC
triethylamine
OCc1ccccc1I
o-iodobenzyl alcohol
ClCc1ccccc1I
title compound
Rendement 100.7%
ClCc1ccccc1I
1-(Chloromethyl)-2-iodobenzene
Rendement 100.7%

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe resulting mixture was extracted with methylene chloride
  2. 2
    SéchageThe methylene chloride layer was dried over anhydrous magnesium sulfate
  3. 3
    Concentrationconcentrated under reduced pressure

Mode opératoire

Methanesulfonyl chloride (2.0 ml, 29 mmol) and triethylamine (3.6 ml, 26 mmol) were added to a solution of o-iodobenzyl alcohol (5.0 g, 21 mmol) in methylene chloride (50 ml) cooled to 0° C., and the mixture was stirred at that temperature for 19 hours. A 5% aqueous sodium hydrogencarbonate solution was added, and the resulting mixture was extracted with methylene chloride. The methylene chloride layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound (5.34 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07897387B2uspto-grants-2011_03