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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68227Generated: October 29, 2026

Citric Acid → 4-Benzylbenzaldehyde

https://huagongshe.com/reaction/68227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
SolventTetrahydrofuranHCID 8028—
Product4-BenzylbenzaldehydeHCID 4988683%

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzyl bromide (41 g, 240 mmol), 4-formylbenzeneboronic acid (28 g, 186.7 mmol), palladium tetrakis triphenyl phosphine (7.9 g, 6.84 mmol) and potassium carbonate (84.7 g, 613 mmol) were combined in tetrahydrofuran (620 mL) and heated at 80° C. under nitrogen for 8 hours. The resulting suspension was allowed to cool to ambient temperature and stirred overnight. The reaction mixture was poured into 10% citric acid (50 mL) and extracted with ethyl acetate (3-fold 50 mL). The combined organic extracts were washed with brine (100 mL) and dried (magnesium sulphate) and the solvent removed in vacuo. The resulting oil was purified by column chromatography on silica gel eluting with ethyl acetate:heptane, (0:1 changing to 1:5, by volume) to give the title compound as a colourless oil, 83% yield, 30.45 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822439B2
Source datasetuspto-grants-2014_09
ORD IDord-88e9b5916c4b4a1eaa9fc78604d5ac0e
Source noteuspto-grants-2014_09