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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461849Generated: October 25, 2026

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

https://huagongshe.com/reaction/461849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-s-triazolo(3,4-b)benzothiazoleHCID 21392831—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064261
Source datasetuspto-grants-1977_12
ORD IDord-713f96a82a5f4e89add3b978835770c7
Source noteuspto-grants-1977_12