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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9167Generated: October 23, 2026

Benzonitrile → (2-Amino-1,3-benzothiazol-6-yl)acetonitrile

https://huagongshe.com/en/reaction/9167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
Reactant4-AminobenzonitrileHCID 13396—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product(2-Amino-1,3-benzothiazol-6-yl)acetonitrileHCID 21298164—

Reaction Conditions

Temperature16 °C

Reaction Steps

2 grams of 4-aminobenzonitrile is dissolved in about 40 mL acetic acid and the solution is cooled to about 16° C. About 3.3 g of potassium thiocyanate is added and the flask is equipped with an addition funnel. The addition funnel is charged with about 2.7 g bromine and about 5 ml 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 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. After drying in vacuo, about 2 grams is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-d0a3bdf85e9b4840981acc50d0208080
Source noteuspto-grants-2006_08