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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111042Generated: November 2, 2026

Trimethyl orthoformate → HCID 72742603, compound

https://huagongshe.com/reaction/1111042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant4-Acetylphenyl isocyanateHCID 99452—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantN-2-Propen-1-ylglycine ethyl esterHCID 10975597—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 72742603HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-d94d92bf8fcb4c2ca7cd96d94acd4e78
Source noteuspto-grants-1990_12