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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9102Erstellt: 24. Oktober 2026

Benzonitrile → 2-Aminobenzothiazole-6-carbonitrile

https://huagongshe.com/de/reaction/9102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzonitrileHCID 7505—
Edukt4-AminobenzonitrileHCID 13396—
EduktBromineHCID 24408—
EduktPotassium thiocyanateHCID 516872—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt2-Aminobenzothiazole-6-carbonitrileHCID 432713967,4%

Reaktionsbedingungen

Temperatur16 °C

Reaktionsschritte

Two grams of 4-aminobenzonitrile was dissolved in about 40 mL acetic acid and the solution was cooled to about 16° C. About 3.3 g of potassium thiocyanate was added and the flask was equipped with an addition funnel. The addition funnel was charged with about 2.7 g bromine and about 5 mL acetic acid. This dark solution was then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 16 hours. The slurry was then drowned into water and filtered. The presscake was washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake was washed well with water. After drying in vacuo, about 2 grams of the title compound was isolated. 1H NMR 6.8 (d, 1H, J=8.7 Hz), 6.9 (br s, 2H), 7.6 (dd, 1H, J=2 Hz, J=8.7 Hz), 8.0 (d, 1H, J=2 Hz), LC/MS 2.34 min, 174 (M−H−), RP-HPLC RT 7.7 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091227B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-5037c9c33a5a49e9b0b5c20797e25f9c
Quellennotizuspto-grants-2006_08