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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009217Generated: October 30, 2026

Toluene → HCID 86761347, compound

https://huagongshe.com/reaction/1009217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactanttert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 86761347HCID 8676134760%

Reaction Conditions

Temperature90 °C

Reaction Steps

307 ml (615 mmol) of an aqueous potassium carbonate solution (2M) are added dropwise to a mixture of 61.5 g (205 mmol) of tert-butyl (3-bromobenzyl)-N-methylcarbamate, 46 g (307 mmol) of 4-formylbenzeneboronic acid and 500 ml of toluene. The reaction medium is subsequently degassed with argon and 7 g (6.2 mmol) of tetrakis(triphenylphosphine)palladium(0) are added. After heating at 90° C. for 24 hours, the reaction medium is poured into water and extracted with ethyl acetate. The organic phase is separated by settling, dried over magnesium sulfate and evaporated. The residue obtained is purified by chromatography on a silica column eluted with a mixture of heptane and ethyl acetate (70/30). After evaporating the solvents, 67 g of tert-butyl (4′-formylbiphenyl-3-yl)methylcarbamate are collected. Yield=60%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973063B2
Source datasetuspto-grants-2011_07
ORD IDord-fc4a8753e3394cbab353bc6d433f2439
Source noteuspto-grants-2011_07