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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1365592Erstellt: 24. Oktober 2026

Benzaldehyde → 2-Phenylbenzothiazole

https://huagongshe.com/de/reaction/1365592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
Edukt2-AminothiophenolHCID 8713—
LösungsmittelO-XyleneHCID 7237—
Produkt2-PhenylbenzothiazoleHCID 13439—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

2-Aminothiophenol (0.856 ml, 8 mmol), benzaldehyde (0.813 ml, 8 mmol), 1 g of an oxidation catalyst and 15 ml of xylene as solvent were charged into a 100 ml three-neck flask, and were stirred at 120° C. for 13 hours under an oxygen atmosphere. The reaction mixture was filtered through Celite, and then the Celite and the oxidation catalyst were washed with ethyl acetate. The filtrate was condensed with a rotary evaporator to yield a solid. The solid was recrystallized from diethyl ether. Resulting colorless crystals were then weighed and the yield thereof was defined as a reaction yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07893004B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-d61abc7cb7ff4475a705cec8cd41030f
Quellennotizuspto-grants-2011_02