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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563922Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 59819988, Verbindung

https://huagongshe.com/reaction/563922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt3-(4-(Trifluoromethyl)phenyl)propionic AcidHCID 3588736—
Edukt2-(5-Methylthiophen-2-yl)ethan-1-amineHCID 14788189—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 59819988HCID 5981998884,5%

Reaktionsschritte

To a solution of 3 g (13 mmol) 4-(trifluoromethyl)hydrocinnamic acid (commercially available) in 30 mL DMF under argon were added 4.7 g (14.37 mmol) TBTU and 11.2 mL (65.3 mmol) N-ethyldiisopropylamine. A solution of 1.85 g (13 mmol) 2-(5-methyl-thiophen-2-yl)-ethylamine in 5 mL DMF was added drop wise over a period of 2 minutes. The mixture was stirred at room temperature for 1 h. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate. The solution was washed with water and with a sat. NaHCO3 solution, dried over Na2SO4, filtered and concentrated in vacuo. The solid was stirred in 30 mL ether, filtered and dried. The mother liquor was concentrated in vacuo and purified on silica eluting with a gradient formed from heptane and ethyl acetate. The product containing fractions were evaporated. 3.75 g (84%) of the title compound was yielded as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067598B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-e2fa1dcde77e410c937eb3ef57d0f3d2
Quellennotizuspto-grants-2011_11