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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9100Generated: October 25, 2026

Benzonitrile → 2-Aminobenzothiazole-6-carbonitrile

https://huagongshe.com/reaction/9100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
Reactant4-AminobenzonitrileHCID 13396—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Aminobenzothiazole-6-carbonitrileHCID 4327139—

Reaction Steps

4-Aminobenzonitrile is dissolved in acetic acid (or a weak protic acid) and the solution is cooled to about 16–30° C., preferably 16–18° C. Potassium thiocyanate is added and the flask is then equipped with an addition funnel. The addition funnel is charged with bromine and acetic acid. This dark solution is then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 12–20 hours, preferrably about 16 hours. The slurry is then drowned into water and filtered. The presscake is washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake is washed well with water to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-6eca5615015f4ce68df2769bea908bce
Source noteuspto-grants-2006_08