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HRID 62260作成日:2026年10月26日

p-Toluenesulfonic acid → (E)-5-bromo-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/62260

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-[(Trifluoromethyl)sulfanyl]benzaldehydeHCID 2777846—
反応物5-Bromo-6-methoxy-1-indanoneHCID 22278718—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
生成物(E)-5-bromo-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-oneHCID 117940068—

反応条件

温度120 °C

反応手順

To a solution of 5-bromo-6-methoxy-2, 3-dihydro-1H-inden-1-one 11 (250 mg, 0.1037 mmol) in benzene was added 4-((trifluoromethyl)thio)benzaldehyde 72 (213 mg, 0.103 mmol). PTSA (395 mg, 0.207 mmol) was added, the reaction mass was stirred at 120° C. for 6 h, then diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude compound 104 and was purified through flash chromatography by using 100-200 mesh silica gel. The compound 104 was eluted at 30% ethyl acetate in hexane to afford yellow coloured solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446047B2
出典データセットuspto-grants-2016_09
ORD IDord-af014326170641db8852a185e3108232
出典メモuspto-grants-2016_09