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HRID 2174840Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2174840

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktPhosphorus oxychlorideHCID 24813—
EduktN,N-bis(1-methylethyl)formamideHCID 75912—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
ProduktN,N,N',N'-tetraisopropylformamidinium chlorideHCID 22491722—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09061973B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-ed997eaac3e342818099877c97432c69
Quellennotizuspto-grants-2015_06