HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242947Generated: October 27, 2026
4-Bromophenol → 1-Bromo-4-[4-(trifluoromethoxy)phenoxy]benzene
https://huagongshe.com/reaction/2242947
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,2,6,6-Tetramethyl-3,5-heptanedione | HCID 70700 | — |
| Reactant | 1-Iodo-4-(trifluoromethoxy)benzene | HCID 2777294 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-Bromo-4-[4-(trifluoromethoxy)phenoxy]benzene | HCID 11530065 | — |
Reaction Steps
A solution of 4-bromophenol (0.173 g) in 4 mL of 1-methyl-2-pyrrolidone under argon atmosphere was treated with 4-(trifluoromethoxy)iodobenzene (0.313 mL), 2,2,6,6-tetramethylheptane-3,5-dione (0.046 mL) and caesium carbonate (0.652 g). The slurry was degassed by bubbling argon for 15 min and copper(I) chloride (0.099 g) was added. The reaction mixture was degassed by bubbling argon for 15 min, then heated to 100° C. under argon for 5 h. The reaction mixture was cooled to room temperature and added dropwise to 30 mL of tert-butyl-methyl-ether. The slurry was filtered and the solids washed with tert-butyl-methyl-ether (3×20 mL). The combined filtrates were washed subsequently with 1N NaOH (50 mL), water (50 mL), 2N HCl (50 mL), 1N HCl (50 mL), water (50 mL) and brine (50 mL). The resulting organic layer was dried over Na2SO4 and concentrated to give a crude product which was purified by column chromatography on silica gel eluting with hexane to afford 0.15 g of the title compound as a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674808B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9356f0c450c64a0caffad2e24111512c |
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| Source note | uspto-grants-2010_03 |
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