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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976284Generated: October 29, 2026

Oxalyl chloride → 4'-(Benzyloxy)[1,1'-biphenyl]-4-carbaldehyde

https://huagongshe.com/reaction/976284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4'-(Benzyloxy)[1,1'-biphenyl]-4-carboxylic acidHCID 14744793—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4'-(Benzyloxy)[1,1'-biphenyl]-4-carbaldehydeHCID 2009990241%

Reaction Steps

Oxalyl chloride (1.72 ml) and dry dimethylformamide (2 drops) were added to a stirred suspension of 4'-benzyloxy-4-biphenylcarboxylic acid (3.04 g) in dry dichloromethane (100 ml). The reaction mixture was stirred for 12 hours at ambient temperature. The mixture was evaporated to dryness. Triphenylphosphine (5.2 g) and bis(triphenylphosphine) copper [I] tetrahydroborate (6.0 g) was added to a solution of the crude product in acetone (150 ml). The mixture was stirred at ambient temperature for 2 hours. The mixture was filtered and the filtrate evaporated. The residue was purified by medium pressure chromatography on silica gel using a mixture of 20% dichloromethane/hexane to remove less polar impurities, followed by ethyl acetate as eluant to give 4'-benzyloxy-4-biphenylcarboxaldehyde as a colourless solid (41% yield), m.p. 122°-123° C., NMR (CDCl3): 5.1 (2H, s), 7.1 (2H, d), 7.4-7.6 (7H, m), 7.7-7.9 (4H, d of d), and 10.0 (1H, s); m/z 289 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612352
Source datasetuspto-grants-1997_03
ORD IDord-6519661ef82f4e16b540033dbd813c4d
Source noteuspto-grants-1997_03