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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875137Generated: October 31, 2026

18-Crown-6 → 3-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]-5-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1875137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactant3-Fluoro-5-(trifluoromethyl)benzonitrileHCID 519037—
Reactant6-Chloro-2-fluoro-3-methylphenolHCID 2773684—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]-5-(trifluoromethyl)benzonitrileHCID 6848740472.2%

Reaction Steps

To a solution of 6-chloro-2-fluoro-3-methylphenol (8.49 g, 52.9 mmol) and 18-crown-6 (13.98 g, 52.9 mmol) in dimethyl sulfoxide (80 ml) was added potassium t-butoxide (20% wt solution in THF) (31.2 g, 55.5 mmol) (31.2 mL) and the mixture was stirred at rt for 30 minutes. Next, 3-fluoro-5-(trifluoromethyl)benzonitrile (10.00 g, 52.9 mmol) was added and the mixture was heated with stirring for 5 hours at 135° C. The reaction mixture was cooled to 0° C., poured into 700 mL water, and the precipitate was filtered off to give the title compound (12.6 g, 38.2 mmol, 72% yield) as a grey solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.10 (s, 1H), 7.80 (s, 1H), 7.74 (s, 1H), 7.39-7.49 (m, 1H), 7.34 (t, 1H), 2.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-aa00006f48ca4fb3ac3d3a51992f386b
Source noteuspto-grants-2012_11