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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129536Erstellt: 25. Oktober 2026

2-Dimethylaminopyridine → HCID 178520426, Verbindung

https://huagongshe.com/reaction/129536

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-DimethylaminopyridineHCID 21885—
EduktCyclohexanepropanoic acidHCID 69702—
EduktPotassium BromideHCID 253877—
EduktTetronic acidHCID 521261—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTriethylamineHCID 8471—
ProduktHCID 178520426HCID 178520426—

Reaktionsschritte

To a solution of 2.0 g of tetronic acid in 40 ml of dry N,N-dimethylformamide was added (at 0° C.) 3.1 ml of triethylamine and 0.81 g of dimethylaminopyridine. After stirring for 5 minutes, 3.4 ml of 3-cyclohexylpropanoic acid was added, followed by 4.6 g of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. After 10 minutes the ice bath is removed and the mixture is allowed to stir overnight. The reaction mixture is quenched with 1N hydrochloric acid and the solution is washed 3 times with hexanes. The combined organic layers are combined, washed with brine, dried over magnesium sulfate and evaporated to give a yellow solid, which is recrystallized from hexanes to give light yellow crystals: m.p. 75°-78° C.; IR (KBr) 2910, 2820, 1750, 1640, 1600 cm-1 ; NMR (CDCl3) δ 0.9-1.8 (1 1H, m), 2.9 (t, 2H, J=6 Hz), 4.7 and 4.5 (s, 2H (tautomers)); MS EI M+ 238.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468774
Quelldatensatzuspto-grants-1995_11
ORD IDord-1b443bad3e6b46e5ab539d1cb4d0abec
Quellennotizuspto-grants-1995_11