HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111007Generated: October 28, 2026
Pyridine → N-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea
https://huagongshe.com/reaction/1111007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86742132 | HCID 86742132 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea | HCID 86744397 | — |
Reaction Steps
A solution of 0.1 mol of p-aminobenzaldehyde ethylene glycol acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of glycine n-propyl 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'-n-propoxycarbonylmethylurea, 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-8b000cacd3dc405b80f383c93bdc69f8 |
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| Source note | uspto-grants-1990_12 |
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