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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | (3-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}-2,5-difluorophenyl)acetonitrile | HCID 66890598 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2,5-Difluoro-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile | HCID 66889713 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872014B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-3083e5d1bc744add928e49e45d2a4969 |
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| Source note | uspto-grants-2011_01 |
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