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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097048Generated: November 1, 2026

Hydrochloric Acid → 4-Dibenzylamino-2,5-dimethylbenzaldehyde

https://huagongshe.com/reaction/1097048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantDibenzyl-(4-iodo-2,5-dimethylphenyl)amineHCID 57461072—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
Product4-Dibenzylamino-2,5-dimethylbenzaldehydeHCID 5746107449.9%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a stirred solution of dibenzyl-(4-iodo-2,5-dimethylphenyl)amine (9.35 g, 21.9 mmol) in toluene (100 mL) under nitrogen at −15° C. was added n-butyllithium in hexanes (1.6 M, 20.5 mL, 32.8 mmol) dropwise via syringe over a 30 min period. The resulting mixture was stirred at −15° C. for 15 min and then N,N-dimethylformamide (1.86 mL, 24.1 mmol) was added dropwise over a 10 min period. After 2 h, aqueous hydrochloric acid (1 M, 46.6 mL) and brine (30 mL) were added and the resulting mixture was stirred for 15 min. The layers were separated and the organic layer was extracted with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-50% DCM in hexanes) to give the title compound (3.60 g, 49% yield) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138345B2
Source datasetuspto-grants-2012_03
ORD IDord-757c991fabce491692bcff5f956e69cc
Source noteuspto-grants-2012_03