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HRID 8418作成日:2026年10月24日

Water → 1,5-Bis[4-[n-[4,6-bis(n-octylamino)-1,3,5-triazin-2-yl]amino]phenoxy]pentane

https://huagongshe.com/ja/reaction/8418

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cyanuric chlorideHCID 7954—
反応物OctylamineHCID 8143—
反応物1,5-Bis(p-aminophenoxy)pentaneHCID 14173—
溶媒TetrahydrofuranHCID 8028—
生成物1,5-Bis[4-[n-[4,6-bis(n-octylamino)-1,3,5-triazin-2-yl]amino]phenoxy]pentaneHCID 2201542945.2%

反応手順

A solution of cyanuric chloride (6.44 grams, 34.9 mmol; obtained from Aldrich Chemical Co.) in dry tetrahydrofuran (50 milliliters) was added dropwise to a solution of 1,5-bis(4-aminophenoxy)pentane (5.00 grams, 17.46 mmol; prepared as described in Part B of Example VIII) in dry tetrahydrofuran (100 milliliters) at −78° C. The mixture was stirred and allowed to warm up to room temperature for 2 hours. Octylamine (23.0 milliliters, 139 mmol; obtained from Aldrich Chemical Co.) was then added and the mixture was stirred at reflux for 3 hours. The mixture was cooled to room temperature, water was added, and the resulting gummy precipitate (like glue) was filtered. The precipitate was dissolved in chloroform and filtered over silica gel. The volatiles were removed under reduced pressure to afford 1,5-Bis[4-[N-[4,6-bis(N-octylamino)-1,3,5-triazin-2-yl]amino]phenoxy]pentane (7.51 grams, 7.88 mmol, 45 percent yield) as a white solid: IR (KBr) 3410, 3279, 2926, 2855, 1575, 1506, 1423, 1369, 1230, 1031, 810 cm−1.

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-9f1ef43dc69b44dd936cbaff8a14f96f
出典メモuspto-grants-2006_08