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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228458Generated: October 26, 2026

Triethylamine → 1-(2-Hex-5-ynoylperhydropyridazinyl)-3,3-dimethylpentane-1,2-dione

https://huagongshe.com/reaction/2228458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant5-Hexynoic acidHCID 143036—
Reactant3,3-Dimethyl-1-perhydropyridazinylpentane-1,2-dioneHCID 69417804—
SolventDichloromethaneHCID 6344—
Product1-(2-Hex-5-ynoylperhydropyridazinyl)-3,3-dimethylpentane-1,2-dioneHCID 1847006563%

Reaction Steps

To a solution of 5-hexynoic acid (0.467 g, 4 mmol) in 10 ml CH2Cl2 was added triethylamine (0.56 ml, 4 mmol), followed by isobutyl chloroformate (0.53 ml, 4 mmol) at 0° C. After stirring for 5 minutes, a solution of 3,3-dimethyl-1-perhydropyridazinyl pentane-1,2-dione (0.424 g, 2 mmol) in 1 ml CH2Cl2 was added. The reaction was gradually warmed up to room temperature. The crude material was subject to silica gel purification to yield final product as clear oil (0.385 g, 63%). 1H NMR (CDCl3, 400 MHz) δ 0.91 (t, 3H, J=7.0); 1.26 (s, 6H); 1.76(m, 8H); 2.28 (m, 2H); 2.50 (m, 2H); 2.88 (m, 2H); 3.60 (m, 1H); 4.50 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417189B1
Source datasetuspto-grants-2002_07
ORD IDord-cff6e2b7d0f34adfafed6d40de6e5289
Source noteuspto-grants-2002_07