HuagongsheHuagongshe Chemistry Print Report · For research reference only
(E)-1-Phenyl-1,3-butadiene → 2-Methyl-3-(2-naphthalenyl)-5-(2-trans-phenylethenyl)-3-(1H-1,2,4-triazol-1-ylmethyl)isoxazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (E)-1-Phenyl-1,3-butadiene | HCID 5371758 | — |
| Reactant | Ethyl acetate pentane | HCID 22335286 | — |
| Reactant | 2-(1H-1,2,4-triazol-1-yl)-N-methyl-1-(2-naphthalenyl)ethanimine N-oxide | HCID 131715728 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-3-(2-naphthalenyl)-5-(2-trans-phenylethenyl)-3-(1H-1,2,4-triazol-1-ylmethyl)isoxazolidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04777263 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-5a5830486caf4ebb96af60b3b8f50333 |
| Source note | uspto-grants-1988_10 |