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Merck

Cyclopropenone catalyzed substitution of alcohols with mesylate ion.

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

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.

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Sigma-Aldrich
甲基磺酸, ≥99.0%
Sigma-Aldrich
甲基磺酸钠, 98%
Sigma-Aldrich
甲基磺酸钾, ≥98.0% (dry substance, T)
Sigma-Aldrich
甲烷磺酸银
Supelco
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Sigma-Aldrich
甲磺酸 溶液, 70 wt. % in H2O
Sigma-Aldrich
甲磺酸 溶液, 4 M (with 0.2% (w/v) tryptamine)