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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671830Generated: October 31, 2026

Pentane → 2,4-Bis(4-tert-butylphenyl)-6-[4'-(2-pyridyl)biphenyl-4-yl]-1,3,5-triazine

https://huagongshe.com/reaction/1671830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
Reactant2-(4-Bromophenyl)pyridineHCID 1515237—
Reactant2-(4-Bromophenyl)-4,6-bis(4-tert-butylphenyl)-1,3,5-triazineHCID 59439787—
ReactantHCID 178418306HCID 178418306—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
Product2,4-Bis(4-tert-butylphenyl)-6-[4'-(2-pyridyl)biphenyl-4-yl]-1,3,5-triazineHCID 6733627287%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under a stream of argon, 3.5 ml of a pentane solution containing 5.2 mmol of tert-butyl lithium was slowly added to 15 ml of tetrahydrofuran cooled to −78° C., and 10 ml of tetrahydrofuran in which 0.61 g of 2-(4-bromophenyl)pyridine was dissolved was further added dropwise to this solution. After stirring at −78° C. for 30 minutes, 1.64 g of dichloro(tetramethylethylenediamine)zinc(II) was added thereto and stirred at −78° C. for 10 minutes and then at room temperature for 2 hours. A 1.00 g portion of 2-(4-bromophenyl)-4,6-bis(4-tert-butylphenyl)-1,3,5-triazine prepared in Reference Example 1 and 0.12 g of tetrakis(triphenylphosphine) palladium(0) were dissolved in 35 ml of tetrahydrofuran and added to this solution, followed by stirring under heating reflux for 13 hours. The reaction solution was concentrated under a reduced pressure and the thus obtained solid was recrystallized from dichloromethane-methanol. The thus obtained crude product was purified by a silica gel column chromatography (eluting solution hexane:dichloromethane=3:2 to 4:3) and then again recrystallized from dichloromethane-methanol to obtain a white solid of the intended 2,4-bis(4-tert-butylphenyl)-6-[4′-(2-pyridyl)biphenyl-4-yl]-1,3,5-triazine (1.00 g, yield 87%). Its melting point and glass transition temperature are shown in Table 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994316B2
Source datasetuspto-grants-2011_08
ORD IDord-1015ed01d1b7473ba892de7e330e69ec
Source noteuspto-grants-2011_08