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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867962Generated: October 26, 2026

(E)-1-Phenyl-1,3-butadiene → 2-Methyl-3-(2-naphthalenyl)-5-(2-trans-phenylethenyl)-3-(1H-1,2,4-triazol-1-ylmethyl)isoxazolidine

https://huagongshe.com/reaction/867962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-1-Phenyl-1,3-butadieneHCID 5371758—
ReactantEthyl acetate pentaneHCID 22335286—
Reactant2-(1H-1,2,4-triazol-1-yl)-N-methyl-1-(2-naphthalenyl)ethanimine N-oxideHCID 131715728—
SolventTolueneHCID 1140—
Product2-Methyl-3-(2-naphthalenyl)-5-(2-trans-phenylethenyl)-3-(1H-1,2,4-triazol-1-ylmethyl)isoxazolidineHCID 14328885—

Reaction Steps

A mixture of 2-(1H-1,2,4-triazol-1-yl)-N-methyl-1-(2-naphthalenyl)ethanimine N-oxide (15.0 g, 0.056 mol) and trans-1-phenyl-1,3-butadiene (11.0 g, 0.084 mol) in 500 ml toluene is heated to 95°-105° C. for 48 hours, then cooled and evaporated to dryness. The resulting oil is decolorized with carbon and purified by flash chromatography on silica gel (eluent comprised of 90% ethyl acetate and 10% hexane by volume) giving two diastereomers. Isomer A (5.66 g) has a melting point of 80°-84° C. (ethyl acetate-pentane). Isomer B (1.64 g) has a melting point 157°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777263
Source datasetuspto-grants-1988_10
ORD IDord-5a5830486caf4ebb96af60b3b8f50333
Source noteuspto-grants-1988_10