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HRID 129537Erstellt: 23. Oktober 2026

Triethylamine → HCID 178520537, Verbindung

https://huagongshe.com/de/reaction/129537

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt2-DimethylaminopyridineHCID 21885—
EduktCyclohexanebutanoic acidHCID 75200—
EduktTetronic acidHCID 521261—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178520537HCID 178520537—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1.0 g (10.0 mmol) of tetronic acid in 30 mL of dry N,N-dimethylformamide at 0° C. is added 1.5 mL (11 mmol) of triethylamine followed by 0.37 g (30 mmol) of 4 dimethylaminopyridine. After stirring at 0° C. for 5 minutes, 2.0 g (11.7 mmol) of 4-cyclohexyl butyric acid is added, followed by 2.25 g (11.7 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide. After 10 minutes, the ice bath is removed and the reaction mixture is allowed to stir overnight. The reaction mixture is quenched with 1N HCl and the solution is washed three times with hexanes. The combined organic layers are washed with water, dried over magnesium sulfate and evaporated. The residue is flash chromatographed on silica gel using 5% methanol/ethyl acetate with 2 mL of acetic acid/liter to give an orange solid: m.p. 38-42° C.; IR (film) 2920, 2840, 1770, 1690, 1660, 1600 cm-1 ; NMR (CDCl3) δ 0.9 (m, 2H), 1.2 (m, 6H), 1.7 (m, 6H), 2.9 (q, J=7 Hz, 2H), 4.6 and 4.7 (s, 2H), 12.1 (bs, 1H); MS (EI): M+ 252.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468774
Quelldatensatzuspto-grants-1995_11
ORD IDord-8fbe33a69b7f439888f617d849ad99cf
Quellennotizuspto-grants-1995_11