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HRID 640669作成日:2026年10月24日

Diethanolamine → 4'-(Bis-(2-hydroxyethyl)-amino)-2,2': 6',2''-terpyridine

https://huagongshe.com/ja/reaction/640669

反応式

関与物質

役割名称HCID仕込み量
反応物DiethanolamineHCID 8113—
反応物4'-Chloro-2,2':6',2''-terpyridineHCID 667748—
触媒Manganese chlorideHCID 26003—
溶媒MethanolHCID 887—
溶媒Sodium HydroxideHCID 14798—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物4'-(Bis-(2-hydroxyethyl)-amino)-2,2': 6',2''-terpyridineHCID 10735597—

反応手順

3.41 g (17.2 mmol) of manganese(II) chloride tetrahydrate and 98 g (0.93 mol) of diethanolamine are added in succession to a mixture of 2.14 g (8 mmol) of 4′-chloro-[2,2′;6′,2″]-terpyridine in 200 ml of methanol. The mixture is heated at reflux for 14 hours, cooled and concentrated. The residue so obtained is stirred in 250 ml of sodium hydroxide solution in acetonitrile/water 1:1 (v/v, pH>12) for 20 hours in air. Acetonitrile is removed using a rotary evaporator and the aqueous portion is extracted three times with chloroform. The organic extract is filtered over sodium sulfate and concentrated. Diethyl ether is added to the residue and the mixture is stirred and filtered, yielding 2-[(2-hydroxy-ethyl)-[2,2′;6′,2″]-terpyridin-4′-yl-amino]-ethanol in the form of a white solid. 1H-NMR (360 MHz, CD3OD): 3.76 (t, J=5.4 Hz, 4 H); 3.85 (t, J=5.4 Hz, 4H); 7.38-7.47 (tm, 2H); 7.69 (s, 2H); 7.94 (dt, J=8.1, 1.8 Hz, 2H); 8.53 (d, J=8.1 Hz, 2H); 8.58-8.65 (dm, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692004B2
出典データセットuspto-grants-2010_04
ORD IDord-2dafbd4d340e413f91e46ebf9f313caa
出典メモuspto-grants-2010_04