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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050706Erstellt: 26. Oktober 2026

1-Butanol → 2,1,3-Benzothiadiazole

https://huagongshe.com/reaction/1050706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-ButanolHCID 263—
EduktSodium CarbonateHCID 10340—
Edukt4,7-Dibromo-2,1,3-benzothiadiazoleHCID 626361—
Edukt4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride)HCID 12166934—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt2,1,3-BenzothiadiazoleHCID 67502—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 4,7-dibromobenzo[2,1,3]thiadiazole (13.2 g, 45 mmol), 4-(N,N-diphenylamino)phenylboronic acid (30.0 g, 104 mmol), a solution of sodium carbonate (21.2 g, 200 mmol) in water (80 mL), tetrakis(triphenylphosphine)palladium(0) (5.0 g, 4.3 mmol), n-butanol (800 mL), and toluene (400 mL) was stirred under argon and heated at 100° C. for 20 hours. After cooling to room temperature, the mixture was diluted with water (600 mL) and stirred for 2 hours. Finally, the reaction mixture was extracted with toluene (2 L), and the volatiles were removed under reduced pressure. The residue was chromatographed using silica gel and hexane/dichloromethane (1:1) as an eluent to give 26.96 g (43.3 mmol, 96%) of 4,7-bis[(N,N-diphenylamino)phenyl)]benzo[2,1,3]thiadiazole (Intermediate M).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382424B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-367db1714ccb420ea4bf501fceef4da4
Quellennotizuspto-grants-2016_07