Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 22154861 | HCID 22154861 | — |
| Reactant | HCID 86744413 | HCID 86744413 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86744414 | HCID 86744414 | — |
Reaction Steps
A solution of 0.1 mol of p-aminobenzaldehyde ethylene glyco acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of isoleucine allyl ester isocyanate and 0.35 mol pyridine in 100 mL THF at room temperature under N2. The reaction mixture is stirred at room temperature for 2 hours. After 2 hours the solvent is removed by rotary evaporator. A solution of 0.11 mmol hydroxylamine hydrochloride and 0.1 mol trimethyl orthoformate in CH3OH is added, and the reaction mixture is heated to reflux under N2 for 1 hour. The reaction mixture is reduced to about 1/4 volume by rotary evaporator, and water is added. The product, N-[4-(hydroxyiminomethyl)phenyl]-N'-[1-(allyloxycarbonyl)-1-methylbutyl]urea, is isolated by filtration and dried in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04977272 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-31e195b929784f2091ade2dd8d619960 |
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| Source note | uspto-grants-1990_12 |
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