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HRID 2217178作成日:2026年10月26日

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 2-(2,4-Dichlorophenyl)-5-methoxybenzoxazole

https://huagongshe.com/reaction/2217178

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物2,4-DichlorobenzaldehydeHCID 13404—
反応物2-Amino-4-methoxyphenolHCID 1419108—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物2-(2,4-Dichlorophenyl)-5-methoxybenzoxazoleHCID 21911684—

反応条件

温度45 °C

反応手順

To a solution of 2-amino-4-methoxyphenol (1 g, 7.1 mmol), a compound of formula (j) in 20 mL MeOH was added (2,4-dichlorophenyl)formaldehyde (1.2 g, 7.1 mmol), a compound of formula (k). The mixture was heated at 45° C. for 12 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in 50 mL dichloromethane. To the solution was added DDQ (1.7 g, 7.8 mmol), and the mixture was allowed to stir at room temperature for 30 minutes. The reaction mixture was then diluted with an additional 30 mL of dichloromethane and washed sequentially with saturated NaHCO3 (2×50 mL) and brine. The organic layer was separated, dried over MgSO4 and concentrated under reduced pressure to yield 2-(2,4-dichlorophenyl)-5-methoxybenzoxazole, a compound of formula (l), which was purified using flash column chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07407960B2
出典データセットuspto-grants-2008_08
ORD IDord-7923245b5dc848aeac326d2b87209248
出典メモuspto-grants-2008_08