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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038272Generated: November 2, 2026

HCID 17841554, compound → HCID 58471577, compound

https://huagongshe.com/reaction/1038272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17841554HCID 17841554—
ReactantAminoammonium hydroxideHCID 44558531—
ReactantHCID 58471583HCID 58471583—
CatalystHCID 178418476HCID 178418476—
Solventtert-Butyl methyl etherHCID 15413—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 58471577HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551359B2
Source datasetuspto-grants-2013_10
ORD IDord-4ebd314b48644dc9bd24bbde8624e18b
Source noteuspto-grants-2013_10