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HRID 1435730생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1435730

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Cyanuric chlorideHCID 7954—
반응물Benzene, 4-chloro-2-iodo-1-methyl-HCID 141766—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물2,4-Dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazineHCID 8582703287.4%

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618968B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-5ca3bce22df24faf937a1ff4ccfbe41a
출처 메모uspto-grants-2009_11