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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097677Generated: October 31, 2026

Triethylamine → HCID 58501887, compound

https://huagongshe.com/reaction/2097677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDecahydroquinolineHCID 92911—
ReactantTriphosgeneHCID 94429—
ReactantHCID 178470429HCID 178470429—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 58501887HCID 58501887—

Reaction Steps

To a solution of decahydroquinoline (10) (1.5 equiv) in dry dichloromethane (0.5 M) under argon was added triethylamine (1.5 equiv) followed by triphosgene (1.5 equiv). The resulting heterogeneous mixture was stirred at room temperature for 15 minutes, concentrated in vacuo. The residue was taken up in dry toluene (0.25 M with respect to amine), treated with dimethylaminopyridine (DMAP) (1.0 equiv) and triazole (9) (1.0 equiv). The resulting mixture was heated to reflux for 1.5 hours, cooled to room temperature and diluted with ethyl acetate and brine, and the aqueous and organic layers were separated. The organic layer was washed with brine, 10% aqueous HCl, then brine, and dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (ethyl acetate/hexanes) to provide ethyl 1-(decahydroquinoline-1-carbonyl)-4-(2-phenoxyphenyl)-1H-1,2,3-triazole-5-carboxylate (11) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450350B2
Source datasetuspto-grants-2013_05
ORD IDord-5ab02473171841cba6c8d6809dd5b177
Source noteuspto-grants-2013_05