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Original Articles

DARSTELLUNG VON PHOSPHONSäUREDIETHYLESTERN DURCH PHOSPHIT-KOPPLUNG VON 1,3-DITHIOL-2-THION-ANELLIERTEN KRONENVERBINDUNGEN

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Pages 283-293 | Received 10 Apr 1996, Accepted 11 Jun 1996, Published online: 04 Oct 2006
 

Abstract

The reaction of the crowned 1,3-dithiole-2-thiones 1 and 2 with triethyl phosphite leads to the tetrathiafulvalenes 3 and 4, as well as 1,3-dithiole-2-yl phosphonate esters 5 and 6. The structure of the phosphonate 6 was confirmed by a single-crystal X-ray structure analysis. Using deuterated triethylphosphites (P(OCH2CD3)3 7, P(OCD2CH3)3, 8) the intramolecular proton transfer yielding the phosphonates was studied.

Synthese der Phosphonsäureester wird gezeigt, daß das zu deren Bildung notwendige Proton von einer CH2-Gruppe des P(OCH2CH3)3 geliefert wird.

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