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HRID 483381Erstellt: 25. Oktober 2026

4-Nitrobenzyl bromide → 4-Benzyl-1-(4-nitrobenzyl)-1,2,4-triazolidin-3,5-dione

https://huagongshe.com/reaction/483381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrobenzyl bromideHCID 66011—
EduktTriazabicyclodeceneHCID 79873—
Edukt4-Benzyl-1,2,4-triazolidine-3,5-dioneHCID 392331—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Benzyl-1-(4-nitrobenzyl)-1,2,4-triazolidin-3,5-dioneHCID 1975262258,6%

Reaktionsschritte

A mixture of 4-benzylurazole (3.8 g, JCS Perkin II, 1975, 1325), p-nitrobenzyl bromide (4.3 g, Aldrich) and polymer-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (P-TBD, 6.3 g, Fluka) in DCM (400 ml) was refluxed under N2 for 24 hours. The P-TBD was filtered off and the filtrate evaporated to leave a gum which was flash chromatographed through a silica column using chloroform/methanol (19:1 v/v) to give the desired product as a solid (3.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05225431
Quelldatensatzuspto-grants-1993_07
ORD IDord-bfc975c33ffb45d99981d0d141bb3d70
Quellennotizuspto-grants-1993_07