HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822250Generated: October 26, 2026
Cesium carbonate → 1-(3-Bromo-phenoxy)-4-chloro-2-phenoxy-benzene
https://huagongshe.com/reaction/1822250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzene, 1-bromo-3-iodo- | HCID 11561 | — |
| Reactant | 2,2,6,6-Tetramethyl-3,5-heptanedione | HCID 70700 | — |
| Reactant | 4-Chloro-2-phenoxyphenol | HCID 12774295 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(3-Bromo-phenoxy)-4-chloro-2-phenoxy-benzene | HCID 57894227 | 40.1% |
Reaction Steps
A solution of 4-chloro-2-phenoxy-phenol (1.65 g, 7.5 mmol), 1-bromo-3-iodobenzene (6.35 g, 22.4 mmol), copper(I) chloride (0.37 g, 3.74 mmol), 2,2,6,6-tetramethyl-3,5-heptanedione (0.345 g, 1.87 mmol), and cesium carbonate (2.93 g, 9 mmol) in NMP (20 mL) is heated to 120° C. The reaction is stirred overnight and cooled to rt. The reaction is quenched with 1N aqueous HCL and extracted with ethyl ether. The organic is washed with brine, dried over sodium sulfate, filtered, and the solvent is removed. The crude is purified by silica gel column chromatography using 5/1 hexanes/ethyl acetate to elute the pure product. The solvent is removed to afford 1.13 g (40%) of the desired product. 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C18H12BrClO2 374, found 375 and 377 (M+1 and M+3, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608639B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-1c85522644d042b78eaa5e86f3f6c207 |
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| Source note | uspto-grants-2009_10 |
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