HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247217Generated: October 31, 2026
p-Aminoacetophenone → HCID 73663829, compound
https://huagongshe.com/reaction/247217
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86740864 | HCID 86740864 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 73663829 | HCID 73663829 | — |
Reaction Steps
A solution of 0.02 mol 4-aminoacetophenone in 40 mL THF is added dropwise to a solution of 0.02 mol of leucine methyl ester isocyanate and 5 mL pyridine in 40 mL THF, and the reaction mixture is stirred for 3 hours. The solvent is then removed by rotary evaporator. The residue is dispersed in 50 mL CH3OH, and 0.022 mol hydroxylamine hydrochloride and 0.06 mol trimethyl orthoformate are added. The reaction mixture is heated to reflux for 1 hour. The solvent is removed by rotary evaporator. Addition of water to the residue results in precipitation of N-[4-(1-hydroxyiminoethyl)phenyl]-N'-(1-methoxycarbonyl-3-methylbutyl)urea, which is then treated with NaOCH3 to adjust the pH to 10. The solution is heated to reflux for 2.5 hours, and the solvent is removed under vacuum. The residue is washed with cold water to yield the crude 3-[4-(1-hydroxyiminoethyl)phenyl]-5-isobutylhydantoin. The hydantoin is purified by recrystallization from CH3OH:H2O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04705864 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-1d188c455a5a4e1a876c6b248ef05ff4 |
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| Source note | uspto-grants-1987_11 |
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