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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082382Generated: October 31, 2026

Water → 2-Azido-1,3-dichloro-5-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2082382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
Reactant4-Amino-3,5-dichlorobenzotrifluorideHCID 141094—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventSulfuric AcidHCID 1118—
Product2-Azido-1,3-dichloro-5-(trifluoromethyl)benzeneHCID 19778409—

Reaction Steps

A solution of sodium nitrite (3.2 g) in concentrated sulphuric acid (22 ml) was added dropwise with cooling to a solution of 2,6-dichloro-4-trifluoromethylaniline (9.3 g) in glacial acetic acid (48 ml). The mixture was stirred at room temperature for half an hour and then cooled to 0°-5°. A solution of sodium azide (2.6 g) in the minimum volume of water was added dropwise with cooling and the mixture stirred at 0°-5° for 1 hour and then at room temperature overnight. The mixture was poured into ice/water, extracted with dichloromethane and the extract worked up in conventional manner to give 1-azido-2,6-dichloro-4-trifluoromethylbenzene, as a red oil. A solution cf this oil (25.6 g) and 2-propyn-1-ol (40 ml) in xylene (80 ml) were stirred under nitrogen and heated under reflux overnight. The mixture was cooled and the solvent was evaporated under reduced pressure. Trituration of the residue with light petroleum (bp 30°-40°) gave a crude material which was purified by filtration through silica to give [1-(2,6-dichloro-4-trifluoromethylphenyl)-1H-1,2,3-triazol-4-yl]methanol, m.p.123°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189053
Source datasetuspto-grants-1993_02
ORD IDord-59e3d714855049d79707bdf75a318a73
Source noteuspto-grants-1993_02