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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349248Generated: October 26, 2026

Potassium Carbonate → 2-(Azidomethyl)-1-methoxy-4-(trifluoromethoxy)benzene

https://huagongshe.com/reaction/349248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium AzideHCID 33557—
Reactant2-Methoxy-5-(trifluoromethoxy)benzyl alcoholHCID 5011246—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(Azidomethyl)-1-methoxy-4-(trifluoromethoxy)benzeneHCID 7139040496%

Reaction Steps

Dissolve (2-methoxy-5-trifluoromethoxy-phenyl)-methanol (4.49 g, 20.2 mmol) in DMF (40 mL) and treat with thionyl chloride (1.65 g, 22.6 mmol). Stir at RT for 2 h, then treat with potassium carbonate (5.57 g, 40.3 mmol), sodium azide (2.35 g, 36.1 mmol), and DMSO (40 mL). Stir the resulting mixture at RT overnight, then pour into water (100 mL) and extract with ether (3×100 mL). Combine the organic phases and wash with water (2×100 mL) and brine (100 mL). Dry the organic layer (MgSO4), filter, and concentrate to give the title compound (4.77 g, 96%) as a colorless oil that may be used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.14 (m, 2H), 6.87 (m, 1H), 4.34 (s, 2H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179804B2
Source datasetuspto-grants-2007_02
ORD IDord-c15d1c975d884f5181e9f470ccee04b6
Source noteuspto-grants-2007_02