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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253259Generated: October 29, 2026

2-Bromoethyl methyl ether → (2,5-Difluoro-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile

https://huagongshe.com/reaction/253259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantPotassium FluorideHCID 522689—
Reactant(3-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}-2,5-difluorophenyl)acetonitrileHCID 66890598—
SolventDimethylformamideHCID 6228—
Product(2,5-Difluoro-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrileHCID 6688971371%

Reaction Steps

To a solution of (3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-2,5-difluorophenyl)acetonitrile (1.22 g, 4.30 mmol) in DMF (10 mL) was added 2-bromoethyl methyl ether (485 μl, 5.16 mmol) and potassium fluoride (0.5 g, 8.6 mmol). The mixture was stirred at room temperature for 15 hrs. The reaction mixture was partitioned between ethyl acetate and water. The aqueous portion was extracted with ethyl acetate. The combined organic portion was washed with brine, dried over sodium sulfate, filtered and concentrated in-vacuo to afford an orange oil, which was purified by column chromatography. Eluting with 30% ethyl acetate in hexanes gave 690 mg, 3.04 mmol (71%) of (2,5-difluoro-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile as a colorless oil. 1H NMR (CDCl3): 6.75-6.69 (m, 2H), 4.17-4.15 (m, 2H), 3.78-3.74 (m, 4H), 3.44 (s, 3H); MS (EI) for C11H11NO2F2: 228 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-3083e5d1bc744add928e49e45d2a4969
Source noteuspto-grants-2011_01