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HRID 1365592作成日:2026年10月25日

Benzaldehyde → 2-Phenylbenzothiazole

https://huagongshe.com/reaction/1365592

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物2-AminothiophenolHCID 8713—
溶媒O-XyleneHCID 7237—
生成物2-PhenylbenzothiazoleHCID 13439—

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893004B2
出典データセットuspto-grants-2011_02
ORD IDord-d61abc7cb7ff4475a705cec8cd41030f
出典メモuspto-grants-2011_02