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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639701Generated: October 29, 2026

1-Azido-4-methoxybenzene → 5-(4-Chloro-2-trifluoromethyl-phenyl)-3-(4-methoxy-phenyl)-3h-[1,2,3]triazol-4-ylamine

https://huagongshe.com/reaction/1639701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Azido-4-methoxybenzeneHCID 75004—
Reactant2-(4-Chloro-2-(trifluoromethyl)phenyl)acetonitrileHCID 3702766—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
Product5-(4-Chloro-2-trifluoromethyl-phenyl)-3-(4-methoxy-phenyl)-3h-[1,2,3]triazol-4-ylamineHCID 2521615784.9%

Reaction Steps

To a stirred and ice-cooled solution of 1-azido-4-methoxy-benzene (0.500 g, 3.3523 mmol) and 4-chloro-2-(trifluoromethyl)phenylacetonitrile (1.104 g, 5.0284 mmol) in absolute ethanol (15 ml), an ice-cooled solution of sodium methoxide (0.217 g, 4.0228 mmol) in absolute ethanol (8 ml) is added drop-wise. The resulting reaction mixture is evaporated and the residue is dissolved in methylene chloride and washed with water, brine, dried over MgSO4, filtered and evaporated to afford ˜1.25 g of crude material as brownish solid. This material is purified by crystallization from methylene chloride and petroleum ether, to obtain the title compound as brown solid (1.05 g, 83% yield). M.p. 159.2-160.2° C. LC-ESI-HRMS of [M+H]+ shows 369.0712 Da. Calc. 369.072998 Da, dev. −4.9 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110588B2
Source datasetuspto-grants-2012_02
ORD IDord-6bddc64f4b5249d89038ea4a40e5976c
Source noteuspto-grants-2012_02