Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | HCID 54163824 | HCID 54163824 | — |
| Product | HCID 20215001 | HCID 20215001 | — |
Reaction Steps
##STR6## 4 mmol of 3-(3-nitrobenzylidene)-4-oxo-butyrolactone (E/Z mixture) and 4.4 mmol of methyl 3-aminocrotonate are suspended in 5 g of tert.-butanol, and the suspension is stirred for 3 hours at 30° C. It is evaporated down at room temperature in a rotary evaporator, and the residue is crystallized with a small amount of methanol. M.p.: 147°-149° C. (from methanol):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04647568 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-abb949e888ac486990b40623257148aa |
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| Source note | uspto-grants-1987_03 |
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