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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477411Generated: October 26, 2026

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

https://huagongshe.com/reaction/1477411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN,N-bis(1-methylethyl)formamideHCID 75912—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN,N,N',N'-tetraisopropylformamidinium chlorideHCID 22491722—

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403766B2
Source datasetuspto-grants-2016_08
ORD IDord-41750638f8554eee8f3e43f759844c41
Source noteuspto-grants-2016_08