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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514738Generated: November 2, 2026

Benzaldehyde → 3-Butyl-5-([E]-styryl)-isoxazole-4-carboxylic acid

https://huagongshe.com/reaction/1514738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantSodium ethoxideHCID 2723922—
Reactant3-Butyl-5-methyl-isoxazole-4-carboxylic acid ethyl esterHCID 66599223—
SolventEthanolHCID 702—
Product3-Butyl-5-([E]-styryl)-isoxazole-4-carboxylic acidHCID 6664373242%

Reaction Steps

To a solution of 3-butyl-5-methyl-isoxazole-4-carboxylic acid ethyl ester (15.0 g, 71.0 mmol) and benzaldehyde (7.2 mL, 71.0 mmol) in ethanol (100 mL) was added sodium ethoxide solution (21% in ethanol, 29.1 mL, 78.0 mmol) and the reaction mixture was stirred at reflux for 2 h, cooled to room temperature and stirred for 17 h. Hydrochloric acid (1 N, 85 mL) was added and the resulting mixture was extracted twice with dichloromethane. The combined phases were washed with brine, dried over sodium sulfate and filtered. The filtrate was concentrated to a bright yellow pasty solid and recrystallized from hot heptane/ethyl acetate to afford the title compound (8.0 g, 42%) as a yellow solid. MS: m/e=270.4 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222246B2
Source datasetuspto-grants-2012_07
ORD IDord-7fb008da5e8c47f58bf5792d2bdb3ef4
Source noteuspto-grants-2012_07