HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413620Generated: October 26, 2026
Trisodium phosphate dodecahydrate → 4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamine
https://huagongshe.com/reaction/413620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trisodium phosphate dodecahydrate | HCID 61473 | — |
| Reactant | 4-Bromo-2,6-difluoroaniline | HCID 610191 | — |
| Reactant | (4-Propylphenyl)boronic acid | HCID 4100861 | — |
| Catalyst | Bis(triphenylphosphine)palladium | HCID 10122028 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamine | HCID 70009956 | 99.5% |
Reaction Steps
348 g trisodiumphosphate dodecahydrate (Merck KGaA, Art. No.106 578) were dissolved in 500 ml of distilled water. Then 8.563 g bis(triphenylphosphine) palladium (Merck KGaA, Art. No. 804 174) and 0.611 g hydaziniumhydroxide (Merck KGaA, Art. No. 804 604) were added. The suspension was stirred for 5 minutes. Then, 126.886 g 4-bromo-2,6-difluoro-aniline, prepared in house, were added. Next 100 g of the p-n-propylphenyl boronic acid, prepared as described above, dissolved in 600 ml dried tetrahydrafurane (Merck KGaA, Art. No.108 107) was added dropwise. The reaction mixture was heated 6 hours under reflux. The organic layer was separated, dried over Na2SO4 and it's solvent evaporated. The isolated crude product (150 g of 4′-n-propyl-3,5-difluoro-biphenyl-4-ylamine was used for the next step of the reaction without further purificatoin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06569505B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-4abd16b979e747879e943d62a7d5e4d7 |
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| Source note | uspto-grants-2003_05 |
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