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Cyclopropenone catalyzed substitution of alcohols with mesylate ion.

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

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Methansulfonsäure, ≥99.0%
Sigma-Aldrich
Natriummethansulfonat, 98%
Supelco
Methansulfonsäurekonzentrat, 0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
Sigma-Aldrich
Kaliummethansulfonat, ≥98.0% (dry substance, T)
Sigma-Aldrich
Silbermethansulfonat
Sigma-Aldrich
Methansulfonsäure -Lösung, 70 wt. % in H2O
Sigma-Aldrich
Methansulfonsäure -Lösung, 4 M (with 0.2% (w/v) tryptamine)