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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530173Generated: October 30, 2026

Diethyl Ether → 2,2'-Difluoro-4''-(3-hydroxypropyl)[1,1';4',1'']-terphenyl-4-ol

https://huagongshe.com/reaction/1530173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 54759098—
ReactantHCID 67195875HCID 67195875—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,2'-Difluoro-4''-(3-hydroxypropyl)[1,1';4',1'']-terphenyl-4-olHCID 67194886—

Reaction Steps

16.5 g (59 mmol) of sodium metaborate octahydrate and 1.3 g (1.8 mmol) of bis(triphenylphosphine)palladium(II) chloride are initially introduced in 150 ml of water and 50 ml of THF, 12.5 g (38.5 mmol) of 3-(4′-bromo-3′-fluorobiphenyl-4-yl)propan-1-ol are added, and a solution of 12.5 g (0.053 mol) of 3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenol in 50 ml of THF is subsequently added dropwise. The batch is heated under reflux overnight, taken up in MTB ether and washed three times with water. The org. phase is dried over sodium sulfate, the solvent is removed in vacuo, and the crude product is recrystallised from toluene/ethyl acetate (9:1), giving 2,2′-difluoro-4″-(3-hydroxypropyl)[1,1′;4′,1″]-terphenyl-4-ol as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090822B2
Source datasetuspto-grants-2015_07
ORD IDord-1944c11e1a81444584f9066aae90dd51
Source noteuspto-grants-2015_07