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HRID 1591599作成日:2026年10月27日

Iodine → 2,4-Dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazine

https://huagongshe.com/reaction/1591599

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Cyanuric chlorideHCID 7954—
反応物Benzene, 4-chloro-2-iodo-1-methyl-HCID 141766—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物2,4-Dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazineHCID 8582703287.4%

反応条件

温度-78 °C

反応手順

Alternatively, to a mixture of magnesium (1.46 g, 60.0 mmol) and tetrahydrofuran (100 ml) was added a small crystal of iodine followed by 4-chloro-2-iodo-toluene (12.62 g, 50 mmol). The mixture was heated under gentle reflux in an argon atmosphere for 6 hours and then cooled to −78° C. A solution of cyanuric chloride (7.84 g, 42.5 mmol) in tetrahydrofuran (45 ml) was added over 25 minutes. After stirring at −78° C. for 1 hour, the mixture was slowly warmed to room temperature and stirred for 16 hours. The reaction mixture, cooled in an ice bath, was quenched by slow addition of hydrochloric acid (1 M, 15 ml). The mixture was diluted with water (150 ml) and extracted with dichloromethane (3×125 ml). The combined extracts was washed with water (150 ml), dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (7:93) to provide 2,4-dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazine (10.2 g, 87% yield) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07291616B2
出典データセットuspto-grants-2007_11
ORD IDord-70e2a9c8b57443fdab1a8176417c65a1
出典メモuspto-grants-2007_11