HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111042Generated: November 2, 2026
Trimethyl orthoformate → HCID 72742603, compound
https://huagongshe.com/reaction/1111042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 4-Acetylphenyl isocyanate | HCID 99452 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | N-2-Propen-1-ylglycine ethyl ester | HCID 10975597 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 72742603 | HCID 72742603 | — |
Reaction Steps
A solution of 0.02 mol N-allylglycine ethyl ester, prepared as described by S. B. Hyeon, I. Nagai, H. Iesaka, T. Kajita, and M. Furushima in European Patent Application No. 181,494, in 40 mL of THF is added dropwise to a solution of 0.02 mol of 4-isocyanatoacetophenone, prepared as described by E. E. Kilbourn, D. L. Peardon, and J. E. Ware in U.S. Pat. No. 3,931,203, and 5 mL of pyridine in 40 mL of 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 of CH3OH, and 0.022 mol of hydroxylamine hydrochloride and 0.06 mol of trimethyl orthoformate are added. The reaction mixture is heated to reflux for 1 hour. The solvent is removed by rotary evaporator to give the product, N-[4-(1-hydroxyiminoethyl)phenyl]-N'-allyl-N'-ethoxycarbonylmethylurea.
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-d94d92bf8fcb4c2ca7cd96d94acd4e78 |
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| Source note | uspto-grants-1990_12 |
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