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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716294Generated: October 31, 2026

4-(p-Tolyloxy)aniline → HCID 68512931, compound

https://huagongshe.com/reaction/1716294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(p-Tolyloxy)anilineHCID 94519—
Reactant5-Bromo-2-methoxypyridine-3-carbaldehydeHCID 1516403—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 68512931HCID 68512931—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-bromo-2-methoxy-pyridine-3-carbaldehyde (0.87 g, 4.03 mmol) in dry MeOH (15 mL) was treated with 4-p-tolyloxy-phenylamine (0.88 g, 4.43 mmol) and reflux for 2.5 h. The solution was cooled to 0° C. and treated slowly with NaBH4 (0.38 g, 10.1 mmol). The reaction stirred at room temperature overnight. Additional NaBH4 (0.38 g, 10.1 mmol) was added and the reaction was continued stirring for additional 6 h. The solvent was removed and the residue was partitioned between CH2Cl2 (20 mL) and water (10 mL). The organic portion was brought to the usual work-up to give a crude material. The product was yielded after chromatography purification (silica gel, 25% EtOAc/hexanes). MS (EI) 399, 401 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-6a3c5efd0a644e5d901c45ad6e36b609
Source noteuspto-grants-2010_09