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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294175Generated: November 3, 2026

Toluene → 2-[4-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinaldehyde

https://huagongshe.com/reaction/1294175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant2-[4-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinonitrileHCID 68885915—
SolventHexaneHCID 8058—
Product2-[4-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinaldehydeHCID 8659156456%

Reaction Steps

To a mixture of 2-[4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinonitrile (4.18 g) and anhydrous toluene (150 mL) was dropwise added a solution (0.95 M, 23.4 mL) of diisobutylaluminum hydride in hexane at −78° C. The reaction mixture was allowed to warm to room temperature with stirring for 1 hr. A saturated aqueous ammonium chloride solution (50 mL) was dropwise added to the mixture and the mixture was further stirred at room temperature for 15 min. Ethyl acetate 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 (2.35 g, 56%) of 2-[4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinaldehyde from a fraction eluted with ethyl acetate-hexane (1:3, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 101-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-8dbc389c4a7742ff9b5555d8eb5c799e
Source noteuspto-grants-2007_07