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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129536Generated: October 26, 2026

2-Dimethylaminopyridine → HCID 178520426, compound

https://huagongshe.com/reaction/129536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
ReactantCyclohexanepropanoic acidHCID 69702—
ReactantPotassium BromideHCID 253877—
ReactantTetronic acidHCID 521261—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178520426HCID 178520426—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468774
Source datasetuspto-grants-1995_11
ORD IDord-1b443bad3e6b46e5ab539d1cb4d0abec
Source noteuspto-grants-1995_11