Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464901Generated: November 2, 2026

Nitrogen → HCID 1782412, compound

https://huagongshe.com/reaction/1464901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-butylbenzeneHCID 521059—
Reactant4-Methoxycarbonylphenylboronic acidHCID 2734369—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
ProductHCID 1782412HCID 178241286%

Reaction Steps

A solution of 1-bromo-4-butylbenzene (100 g, 0.472 mol), 4-(methoxycarbonyl)phenylboronic acid (82.0 g, 0.456 mol), 2 M Na2CO3 (150 g, 1.42 mol) in toluene/EtOH (900 mL/300 mL) was degassed with N2 three times, then Pd(PPh3)4 (27.2 g, 23.6 mmol) was added. The resulting mixture was degassed with N2 three times and then heated to reflux for 5 hrs. After TLC showed the reaction was complete, toluene and EtOH was removed under vacuum. The residue was extracted with EA (30 mL×3). The combined organic layers were washed with brine, dried with Na2SO4. The solvent was removed to give the crude product. The crude product was purified by column chromatography on silica gel eluted with PE, PE:EA (150:1). The solvent was removed to give methyl 4-(4-butylphenyl)benzoate (105 g, yield: 86.0%), as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999922B2
Source datasetuspto-grants-2015_04
ORD IDord-2547d5a67eee4a36a9d8e1a80a4a5e19
Source noteuspto-grants-2015_04