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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 588287생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/588287

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Phosphorus oxychlorideHCID 24813—
반응물N,N-bis(1-methylethyl)formamideHCID 75912—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물N,N,N',N'-tetraisopropylformamidinium chlorideHCID 22491722—

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09227934B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-b3d399308a7b4c489319be48bc3ceea4
출처 메모uspto-grants-2016_01