DABSO

CAS 119752-83-9, Cat. No EN300-321062
Reagent SO2 source

DABSO
EN300-321062

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DABSO, is a bench-stable colorless solid suitable for use in organic synthesis as a replacement for gaseous sulfur dioxide[1]. The complex can be combined with Grignard reagents to form sulfinates, which can then be converted in situ to a series of sulfonamides[1], [2]. Alternatively, a reaction with anilines and iodine leads to the formation of a series of sulfamides. Cheletropic addition between DABSO and 2,3-dimethylbutadiene provides the corresponding sulfolene[2]. This versatile compound finds application as an efficient reagent, offering enhanced convenience and control in the synthesis of sulfinates, sulfonamides, and related derivatives.

Synonyms: 1,4-Diazabicyclo[2.2.2]octane sulfur dioxide complex, 1,4-Diazabicyclo[2.2.2]octane-1,4-diium-1,4-disulfinate, 1,4-Diazobicyclo[2.2.2]octane-bis(sulfur dioxide) adduct, 1,4, Diazoniabicyclo[2.2.2]octane-1,4-disulfinate, DABCO bis(sulfur dioxide) adduct, DABCO-bis(sulfur dioxide), DABSO, 1,4-diazabicyclo[2.2.2]octane-1,4-diium-1,4-disulfinate

Selected publication

  1. DABCO-Bis (Sulfur Dioxide), DABSO, as a Convenient Source of Sulfur Dioxide for Organic Synthesis: Utility in Sulfonamide and Sulfamide Preparation.

    Woolven H.; González-Rodríguez C.; Marco I.; Thompson A. L.; Willis M. C. Org Lett 2011, 13 (18), 4876–4878. DOI: 10.1021/ol201957n

  2. 1,4-Disulfino-1,4-Diazabicyclo [2.2.2]Octane, Bis(Inner Salt).

    Deeming A. S.; Willis M. C.; Lu T.; Xiang Y.; Wu J. Encyclopedia of Reagents for Organic Synthesis 2018, 1–15. DOI: 10.1002/047084289X.rn01912

 

 

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