Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Z)-Benzaldehyde oxime | HCID 12143 | — |
| Reactant | Methyl hydrogen prop-2-en-1-ylcarbonimidate | HCID 186042 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12889667 | HCID 12889667 | — |
Reaction Steps
A 24 g. portion of benzaldoxime was chlorinated, isolated and dissolved in diethyl ether. The solution was cooled to 15° C., and 46 g. of methyl allylcarbamate was added. Sixty ml. of triethylamine was then added dropwise, keeping the temperature below 20° C. The mixture was stirred for 3 hours, and filtered. The filtrate was evaporated to dryness, and the residue was washed with water and filtered again. The solids were identified as 32 g. of product, m.p. 102°-103° C., NMR singlets at 3.63 and 5.48 ppm., multiplets at 2.82-3.80, 4.57-5.08, 7.13-7.50 and 7.45-7.77 ppm.
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-f3849fc1a3da4249ba44783383b682ee |
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| Source note | uspto-grants-1981_08 |
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