Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635755Generated: November 1, 2026

Toluene → Diethyl 2-(4'-hexyloxyphenyl)terephthalate

https://huagongshe.com/reaction/1635755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hexyloxyphenylboronic AcidHCID 3682148—
ReactantDiethyl 2-bromoterephthalateHCID 11033938—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductDiethyl 2-(4'-hexyloxyphenyl)terephthalateHCID 11069361—

Reaction Conditions

Temperature85 °C

Reaction Steps

Diethyl bromoterephthalate (30.1 g, 100 mmol), K2CO3 (27.6 g, 200 mmol) and 140 ml of toluene and 140 ml of H2O were placed in a reaction vessel and argon was passed in for 30 minutes. 4-hexyloxyphenylboronic acid (26.7 g, 120 mmol) (cf. B1) and Pd(PPh3)4 (1.16 g, 1 mmol) were subsequently added under protective gas. The yellow-green, turbid mixture was stirred vigorously under a blanket of protective gas at an internal temperature of 85° C. After 7 hours, the reaction was complete. 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 product was obtained as a yellowish brown oil in sufficient purity (about 85%): 44.7 g (1112%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509507B2
Source datasetuspto-grants-2003_01
ORD IDord-66b34cb7630745c3b2444332cd92801d
Source noteuspto-grants-2003_01