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STUDIES ON ORGANOPHOSPHORUS COMPOUNDS. PART VI. THE REACTION OF ALKOXIDES WITH 2,4-BIS(4-METHOXYPHENYL)-1,3,2,4-DITHIADIPHOSPHETANE 2,4-DISULFIDE (LR). A NEW APPROACH FOR THIO-INEZIN

Pages 293-296 | Received 17 Feb 1986, Accepted 05 May 1986, Published online: 24 Feb 2007
 

Abstract

Sodium alkoxide, a hard nucleophile, reacts with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (LR) on phosphorus to give O-alkyl S-sodium-(4-methoxyphenyl) phosphonothiolothionate 5 as an intermediate. Compound 5 reacts with benzyl (or benzoyl) chloride to give good yields of O-alkyl S-benzyl (benzoyl) (4-methoxy-phenyl)phosphonothiolothionate (6a–e).

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