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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129537Generated: October 25, 2026

Triethylamine → HCID 178520537, compound

https://huagongshe.com/reaction/129537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantCyclohexanebutanoic acidHCID 75200—
ReactantTetronic acidHCID 521261—
SolventDimethylformamideHCID 6228—
ProductHCID 178520537HCID 178520537—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468774
Source datasetuspto-grants-1995_11
ORD IDord-8fbe33a69b7f439888f617d849ad99cf
Source noteuspto-grants-1995_11