HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038272Generated: November 2, 2026
HCID 17841554, compound → HCID 58471577, compound
https://huagongshe.com/reaction/1038272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 17841554 | HCID 17841554 | — |
| Reactant | Aminoammonium hydroxide | HCID 44558531 | — |
| Reactant | HCID 58471583 | HCID 58471583 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 58471577 | HCID 58471577 | — |
Reaction Steps
A mixture of 2.60 g (14.3 mmol) of 2-fluoro-4-propylbenzeneboronic acid, 7.0 g (13.1 mmol) of 4′-[(4-bromo-2,6-difluorophenyl)difluoromethoxy]-3,5,2′-trifluoro-4-trifluoromethylbiphenyl, 0.30 g (0.42 mmol) of bis(triphenyl-phosphine)palladium(II) chloride and 2.80 g (10.1 mmol) of sodium metaborate octahydrate is initially introduced in 40 ml of THF/water=3:1. 0.02 ml (0.4 mmol) of hydrazinium hydroxide is added, and the mixture is refluxed for 20 h. After cooling, the batch is diluted with MTBE, and the mixture is washed with water. The organic phase is separated off, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with water. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 4-[difluoro(3,5,2′-trifluoro-4′-propyl-biphenyl-4-yl)methoxy]-6,3′,5′-trifluoro-4′-trifluoromethylbiphenyl as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551359B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-4ebd314b48644dc9bd24bbde8624e18b |
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| Source note | uspto-grants-2013_10 |
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