HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067704Generated: November 1, 2026
4-Bromodiphenyl Ether → HCID 59317894, compound
https://huagongshe.com/reaction/2067704
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromodiphenyl Ether | HCID 7565 | — |
| Reactant | 1-Bromo-2-nitrobenzene | HCID 11341 | — |
| Reactant | Butyl Acetate | HCID 31272 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 59317894 | HCID 59317894 | — |
Reaction Steps
The same reaction was performed as in Example 148 except for using, instead of the 2-bromonitrobenzene, 4-bromodiphenyl ether. That is, to a solution of the compound obtained at Example 142 (60 mg) in n-butyl acetate (4.5 ml) were added 4-bromodiphenyl ether (93 mg), palladium acetate (4.3 mg), 2-(di-tert-butylphosphino)biphenyl (11.4 mg) and tripotassium phosphate (161 mg), and the mixture was heated and stirred at 120° C. for 24 hours. The reaction mixture was cooled to room temperature, then the insolubles were filtered off, the filtrate was distilled off in vacuo and the residue obtained was purified by silica gel column chromatography (hexane:ethyl acetate=9:1 to 3:2) to afford the above-identified compound (77 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293781B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5a77d989a9cf453ba212aafcd02e77e8 |
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| Source note | uspto-grants-2012_10 |
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