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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365592Generated: October 25, 2026

Benzaldehyde → 2-Phenylbenzothiazole

https://huagongshe.com/reaction/1365592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant2-AminothiophenolHCID 8713—
SolventO-XyleneHCID 7237—
Product2-PhenylbenzothiazoleHCID 13439—

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893004B2
Source datasetuspto-grants-2011_02
ORD IDord-d61abc7cb7ff4475a705cec8cd41030f
Source noteuspto-grants-2011_02