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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656017Generated: October 29, 2026

Triethylamine → HCID 21802382, compound

https://huagongshe.com/reaction/1656017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-3-ethylbenzoxazolium tetrafluoroborateHCID 2724240—
ReactantHCID 21802383HCID 21802383—
SolventDichloromethaneHCID 6344—
ProductHCID 21802382HCID 21802382—

Reaction Steps

To a stirred solution of 0.40 g (1.3 mmols) of N-[2-(4-chlorophenyl)-1-(1,2,4-triazol-1-yl)-2-hexyl]formamide in 5 mL of methylene chloride under nitrogen was added 0.45 mL (3.26 mmols) of triethylamine. To this mixture was added a slurry of 0.439 g (1.63 mmols) of 3-ethyl-2-chlorobenzoxazolium tetrafluoroborate, which was weighed out under a nitrogen atmosphere, in 5 mL of methylene chloride. The reaction mixture was then allowed to stir at room temperature for 12 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate. The combined organic layers were washed once with 10% hydrochloric acid, brine, and dried over magnesium sulfate. Removal of solvents gave a crude oil which was purified by column chromatography (Merck 60 silica gel, ethyl acetate/hexane) to give 0.20 g (52%) of a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252594
Source datasetuspto-grants-1993_10
ORD IDord-e4719c960f974106af2b92994f759c02
Source noteuspto-grants-1993_10