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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870116Generated: October 30, 2026

2,6-Di-tert-butylphenol → HCID 66586998, compound

https://huagongshe.com/reaction/870116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butylphenolHCID 31405—
ReactantPotassium FluorideHCID 522689—
Reactant2,7-Dibromo-9,9-bis(6-bromohexyl)-9H-fluoreneHCID 21867930—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 66586998HCID 66586998—

Reaction Conditions

Temperature100 °C

Reaction Steps

A flask with a stirring bar was charged with a mixture of compound 1 (1.000 g, 1.54 mmol), PdCl2(PPh3)2 (0.0588 g, 0.065 mmol), a few crystals of 2,6-ditert-butylphenol, and toluene (15.0 mL). The mixture was heated to 100° C. under nitrogen, and tributylvinyltin (1.125 g, 3.534 mmol) was added dropwise. The mixture was further heated for 23 hours. It was subsequently diluted with 60 mL of ether and treated with KF solution (˜10%). The mixture was stirred for 20 hours and followed by filtration to remove the insoluble solid. The organic layer was washed with water and dried over anhydrous MgSO4. After removal of the solvent, the residue was purified by column chromatography with n-hexane as eluent to afford 0.650 g of compound 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969509B2
Source datasetuspto-grants-2015_03
ORD IDord-4bbe3177a8784ef1a311010b986c19fd
Source noteuspto-grants-2015_03