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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233734Generated: October 30, 2026

Pyridine → 2-(2H-Benzotriazol-2-yl)ethan-1-amine

https://huagongshe.com/reaction/233734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 817804HCID 817804—
SolventDiethyl EtherHCID 3283—
Product2-(2H-Benzotriazol-2-yl)ethan-1-amineHCID 1048720244,791.699%

Reaction Conditions

Temperature-50 °C

Reaction Steps

4.70 g Of the 2-(2-benzotriazolyl)ethanol (28.8 mmol) was dissolved in 200 ml diethyl ether and 2.28 g pyridine (28.8 mmol) was added. The mixture was cooled to -50° C., and 8.18 g triflic anhydride (29 mmol) was added. The mixture was removed from the cooling bath, and was allowed to reach room temperature. The mixture was filtered under dry conditions and added to a cold -40° C. solution of ca 150 ml ammonia in 50 ml diethyl ether. This mixture was allowed to reach room temperature, and ether was removed. 50 ml 2M HCl was added, and this mixture was washed with methylene chloride. The aqueous phase was made basic by addition of 50 ml 25% sodium hydroxide and extracted with 3×25 ml methylene chloride. Evaporation of the solvent gave 2.10 g 2-(2-benzotriazolyl)ethylamine (12.9 mol). This amine was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593993
Source datasetuspto-grants-1997_01
ORD IDord-949a319935e546c5963c3f34f22892aa
Source noteuspto-grants-1997_01