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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 461849Erstellt: 24. Oktober 2026

N-bromobutanimide → 3-Bromo-s-triazolo(3,4-b)benzothiazole

https://huagongshe.com/de/reaction/461849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt3-Bromo-s-triazolo(3,4-b)benzothiazoleHCID 21392831—

Reaktionsschritte

s-Triazolo(3,4-b)benzothiazole (6.4 grams; 0.0366 mole) was slurried with 200 milliliters of carbon tetrachloride, with stirring, at room temperature, and then heated. N-Bromosuccinimide (6.8 grams; 0.0366 mole plus 5 percent) was added and the solution refluxed and a pinch of azobisisobutylnitrile added to initiate the reaction. Subsequently the reaction mixture was filtered to separate blackish crystals, which were washed with carbon tetrachloride. The carbon tetrachloride was removed by evaporation, to yield a purple solid. This was chromatographed on a column packed with silica gel and eluted with ethyl acetate. The second portion was analyzed by elemental analysis and NMR, which confirmed its identity as the expected 3-bromo-s-triazolo(3,4-b)benzothiazole, m.p., 166°-7° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04064261
Quelldatensatzuspto-grants-1977_12
ORD IDord-713f96a82a5f4e89add3b978835770c7
Quellennotizuspto-grants-1977_12