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HRID 8419作成日:2026年10月24日

Dibromomethane → 1,1-Bis[4-[n,n-bis[4,6-dichloro-1,3,5-triazin-2-yl]amino]phenoxy]methane

https://huagongshe.com/ja/reaction/8419

反応式

関与物質

役割名称HCID仕込み量
反応物DibromomethaneHCID 3024—
反応物Cyanuric chlorideHCID 7954—
反応物Sodium hydrideHCID 24758—
反応物4-[(4-Aminophenoxy)methoxy]anilineHCID 60234—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Bis[4-[n,n-bis[4,6-dichloro-1,3,5-triazin-2-yl]amino]phenoxy]methaneHCID 2201544016%

反応条件

温度60 °C

反応手順

Cyanuric chloride (11.473 grams, 62.2 mmol) in dry tetrahydrofuran (50 milliliters) was added to a solution of 1,1-bis(4-aminophenoxy)methane (3.58 grams, 15.55 mmol; prepared as described in Part B of Example VIII except that 1,1-dibromomethane was used instead of 1,5-dibromopentane) in dry tetrahydrofuran (175 milliliters) at −10° C. The mixture was stirred for 10 minutes and sodium hydride (3.75 grams, 93.3 mmol) was added dropwise. The mixture was then heated to 60° C. for 16 hours and subsequently filtered on CELITE. The volatiles were removed under reduced pressure and the crude solid was purified on silica gel using a mixture of AcOEt/hexane (3:7, v/v) as eluant to afford pure 1,1-bis[4-[N,N-bis[4,6-dichloro-1,3,5-triazin-2-yl]amino]phenoxy]methane (2.10 grams, 2.55 mmol, 16 percent yield) as a white solid. Chromatography with silica gel is believed to be responsible for the low yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087752B2
出典データセットuspto-grants-2006_08
ORD IDord-15b09eaac7d0451581148c6eef1c9bd2
出典メモuspto-grants-2006_08