Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Butene, 1-isothiocyanato- | HCID 544291 | — |
| Reactant | N-hydroxybenzenecarboximidoyl chloride | HCID 2756315 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12889639 | HCID 12889639 | — |
Reaction Steps
A 23 g. portion of α-chlorobenzaldoxime, prepared as in Example 1 above, was combined with 17 g. of crotylisothiocyanate in 300 ml. of diethyl ether. The solution was cooled to 15° and 40 ml. of triethylamine in 100 ml. of tetrahydrofuran was added dropwise. The mixture was stirred for 24 hours at 15°, and was then filtered. The filtrate was washed with water, and evaporated to dryness. The residue was dissolved in chloroform, and chromatographed over a column (2.5 cm. diameter by 8 meters long) of polystyrene gel beads. The eluate was evaporated to dryness, and the residue was recrystallized from diisopropyl etherhexane. The product was identified as 10 g. of 5-(2-isothiocyanatoethyl)-3-phenyl-2-isoxazoline, m.p. 54°-56°. The microanalytical results were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04283403 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-3c2e34f3a5bb4aeb940a8d8a76b748ca |
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| Source note | uspto-grants-1981_08 |
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