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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635761Generated: November 1, 2026

Toluene → 2,5-Dimethyl-4'-hexyloxybiphenyl

https://huagongshe.com/reaction/1635761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBenzene, 2-bromo-1,4-dimethyl-HCID 11121—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hexyloxyphenylboronic AcidHCID 3682148—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2,5-Dimethyl-4'-hexyloxybiphenylHCID 18676619—

Reaction Conditions

Temperature85 °C

Reaction Steps

Bromo-p-xylene (8.3 g, 45 mmol) (cf. A1 a)), K2CO3 (12.4 g, 90 mmol), 70 ml of toluene and 70 ml of H2O were placed in a reaction vessel and argon was passed in for 30 minutes. 4-hexyloxyphenylboronic acid (10 g, 45 mmol) and Pd(PPh3)4 (0.65 g, 0.56 mmol) were subsequently added under protective gas. The yellow-green, turbid mixture was stirred vigorously under a blanket of protective gas for about 20 hours at an internal temperature of 85° C. After phase separation, the organic phase was shaken with dilute HCl/H2O (until neutral). The aqueous phase was shaken with toluene and the organic phases were combined. After filtering off any palladium residues, the solution was evaporated. The crude product was purified by distillation under reduced pressure: the product was obtained as a yellow oil (boiling point: 117°-125° C./0.08 mbar): 10.3 g (81%). Purity>95% (1H-NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509507B2
Source datasetuspto-grants-2003_01
ORD IDord-28d132ad7a944018b7dc1ca657b3b54a
Source noteuspto-grants-2003_01