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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294133Generated: November 4, 2026

Toluene → 2-[4-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridinecarbaldehyde

https://huagongshe.com/reaction/1294133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant2-({4-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]benzyl}oxy)nicotinonitrileHCID 68886220—
SolventHexaneHCID 8058—
Product2-[4-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridinecarbaldehydeHCID 8659157576%

Reaction Steps

To a mixture of 3-cyano-2-[4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]pyridine (8.42 g) and anhydrous toluene (300 mL) was dropwise added a solution (1M, 46.6 mL) of diisobutylaluminum hydride in hexane at −78° C. The reaction mixture was allowed to warm to room temperature over 1 hr with stirring. A saturated aqueous ammonium chloride solution (70 L) was dropwise added to the mixture, and the mixture was further stirred at room temperature for 30 min. Ethyl acetate (300 mL) was added to the mixture and, after stirring the mixture at room temperature for 30 min., insoluble materials were filtered off. The filtrate, was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The obtained residue was subjected to silica gel column chromatography to give crystals (6.49 g, 76%) of 2-[4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridinecarbaldehyde from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 97-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-8abacef81581491b9cec5c2a59fd8f16
Source noteuspto-grants-2007_07