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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475245Generated: October 26, 2026

Allyl bromide → 5-(1-(3-(allyloxy)benzyl)-5-methyl-1H-1,2,4-triazol-3-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1475245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactantt-Bu4NHSO4HCID 9927882—
ReactantHCID 86711921HCID 86711921—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(1-(3-(allyloxy)benzyl)-5-methyl-1H-1,2,4-triazol-3-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazoleHCID 8671193792.7%

Reaction Steps

A solution of 3-((5-methyl-3-(3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazol-5-yl)-1H-1,2,4-triazol-1-yl)methyl)phenol (Example 59; 140 mg, 0.33 mmol) in DCM (5 mL), was added to a mixture of 3-bromoprop-1-ene (60 mg, 0.5 mmol), K2CO3 (138 mg, 1.0 mmol) and t—Bu4NHSO4 (113 mg, 0.33 mmol) in H2O (5 mL). The mixture was stirred at RT for 16 h, then diluted with H2O (50 mL) and extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (20 mL), dried over Na2SO4, filtered and concentrated under reduced pressure; the residue was purified by silica gel chromatography (Petroleum ether:EtOAc=5:1 to 2:1) to give the title compound (140 mg, 91%) as a white solid. MS (ES+) C22H18F3N5O3 requires: 457. found: 458 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018380B2
Source datasetuspto-grants-2015_04
ORD IDord-20aa59f0b47b4c6aa318cdef0acfa24b
Source noteuspto-grants-2015_04