Accéder au contenu
MilliporeSigma

Cyclopropenone catalyzed substitution of alcohols with mesylate ion.

Organic letters (2012-12-15)
Eric D Nacsa, Tristan H Lambert
RÉSUMÉ

The cyclopropenone catalyzed nucleophilic substitution of alcohols by methanesulfonate ion with inversion of configuration is described. This work provides an alternative to the Mitsunobu reaction that avoids the use of azodicarboxylates and generation of hydrazine and phosphine oxide byproducts. This transformation is shown to be compatible with a range of functionality. A cyclopropenone scavenge strategy is demonstrated to aid purification.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Acide méthanesulfonique, ≥99.0%
Sigma-Aldrich
Sodium methanesulfonate, 98%
Supelco
Acide méthane sulfonique solution, 0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
Sigma-Aldrich
Potassium methanesulfonate, ≥98.0% (dry substance, T)
Sigma-Aldrich
Silver methanesulfonate
Sigma-Aldrich
Acide méthane sulfonique solution, 70 wt. % in H2O
Sigma-Aldrich
Acide méthane sulfonique solution, 4 M (with 0.2% (w/v) tryptamine)