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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987506Generated: November 1, 2026

Ethyl Bromide → HCID 178462785, compound

https://huagongshe.com/reaction/1987506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
Reactant1H-1,2,3-triazol-1-amineHCID 3825723—
SolventAcetonitrileHCID 6342—
ProductHCID 178462785HCID 178462785520.7%

Reaction Steps

In a 100 ml glass reactor, equipped with a magnetic stirrer was placed 2.00 g (3.8 mmoles) of 1-amino-1,2,3-triazole (1) and dissolved in 40 ml of acetonitrile. To the reaction mixture was added 12.05 g (110.5 mmoles) of ethyl bromide and the reactor was sealed. The reaction mixture was stirred vigorously at 45° C. until all 1-amino-1,2,3-triazole was consumed. As the reaction progressed, white crystals of 1-amino-3-ethyl-1,2,3-triazolium bromide (2b) precipitated. The reaction mixture was cooled down to room temperature. The product salt was filtered and washed with several aliquots (50 ml total) of diethyl ether. The mother liquor was concentrated by distillation under reduced pressure, resulting in a second crop of crystals that were filtered, washed with diethyl ether, combined with the first crop and dried under high vacuum, resulting in a good yield of 3.82 g (83%) of 1-amino-3-ethyl-1,2,3-triazoliumbromide (2b), mp 117-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550601B1
Source datasetuspto-grants-2009_06
ORD IDord-d0d84cccbc8e413ab0cb204f9635d956
Source noteuspto-grants-2009_06