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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58983Generated: October 29, 2026

Nitrogen → [1,1'-Biphenyl]-3,5-dicarboxaldehyde

https://huagongshe.com/reaction/58983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromobenzene-1,3-dicarbaldehydeHCID 14383230—
CatalystTriphenylphosphineHCID 11776—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product[1,1'-Biphenyl]-3,5-dicarboxaldehydeHCID 1419932774%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 5-bromoisophthaldehyde (40.0 g, 187.8 mmol), phenylboronic acid (22.9 g, 187.8) and potassium carbonate (64.8 g, 469.5 mmol) in DME/H2O (5:1 600 mL) was purged with N2 for 5 min. Tetrakispalladium triphenylphosphine (1.1 g mg, 0.9 mmol) was added and the reaction mixture was heated to 90° C. and stirred for 16 h. The reaction mixture was cooled, filtered through a pad of celite and the solvent evaporated under reduced pressure. Purification by column chromatography (10% EtOAc/hexanes) afforded the desired product (74%, 29.1 g) as a tan solid. 1H NMR (300 MHz, CDCl3) δ ppm 10.18 (s, 2H), 8.37 (d, J 1.2 Hz, 2H), 8.35 (t, J=1.5 Hz, 1H), 7.70-7.66 (m, 2H), 7.55-7.43 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439433B2
Source datasetuspto-grants-2016_09
ORD IDord-4a1481daaf7148a49eaea6a4f999b1b3
Source noteuspto-grants-2016_09