HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661104Generated: October 27, 2026
Dimethylformamide → 4-Bromo-2-methoxy-1-(trifluoromethyl)benzene
https://huagongshe.com/reaction/661104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromo-2-fluorobenzotrifluoride | HCID 2782904 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | 4-Bromo-2-methoxy-1-(trifluoromethyl)benzene | HCID 68990569 | 46% |
Reaction Steps
To a 250 mL round-bottomed flask was added 4-bromo-2-fluoro-1-(trifluoromethyl)benzene (12 mL, 50 mmol) and DMF (4.0 mL, 50 mmol). The solution was stirred at 0° C. and treated with sodium methoxide (4 g, 75 mmol). The reaction mixture was stirred at room temperature for 30 minutes and 60° C. for 2 hours. The resulting milky suspension was quenched with ice at 0° C. and the separated aqueous layer was extracted with EtOAc (3×50 mL). The combined organic layers were washed with saturated sodium chloride (1×25 mL), dried over Na2SO4, and concentrated to give the crude residue which was purified with flash column chromatography ((5%→20% EtOAc in hexane) to provide 4-bromo-2-methoxy-1-(trifluoromethyl)benzene (5.80 g, 46% yield) as a light yellow oil. m/z (%): 256.1.2 (100%, M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084479B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2b7e295d88e849f2a5d98d3f6a2e4997 |
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| Source note | uspto-grants-2011_12 |
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