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HRID 588287作成日:2026年10月26日

Diisopropylamine → N,N,N',N'-tetraisopropylformamidinium chloride

https://huagongshe.com/reaction/588287

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Phosphorus oxychlorideHCID 24813—
反応物N,N-bis(1-methylethyl)formamideHCID 75912—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物N,N,N',N'-tetraisopropylformamidinium chlorideHCID 22491722—

反応条件

温度0 °C

反応手順

A mixture of phosphorus oxychloride (10.58 g) and diethyl ether (50 ml) is stirred at 0° C. for 10 min. Diisopropylformamide (8.91 g) in diethyl ether (20 ml) is then added drop-wise over a period of 10 min. The resulting mixture is then stirred at room temperature for 30 min. The formed precipitate is allowed to settle and the supernatant removed. Dichloromethane (60 mL) is then added to the mixture. Diisopropylamine (6.98 g) in dichloromethane (20 ml) is then added drop-wise at 0° C. over 10 min. The mixture is then warmed at room temperature and stirred for a further 1.5 h. Diethyl ether (30 ml) is added and the resulting precipitate is removed by filtration. The mother liquor is concentrated in vacuo. Acetone (30 ml) is added and the mixture filtered. The mother liquor is then concentrated in vacuo and subsequently is crystallised with diethyl ether (30 ml) to give N,N,N′,N′-tetraisopropylformamidinium chloride (18, R6=iPr, R7=iPr). 1H NMR (DMSO-d6), 7.49 (1H), 4.15-3.95 (4H), 1.33 (12H), 1.31 (12H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227934B2
出典データセットuspto-grants-2016_01
ORD IDord-b3d399308a7b4c489319be48bc3ceea4
出典メモuspto-grants-2016_01