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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607842Generated: November 2, 2026

Trimethyl orthoformate → HCID 72742603, compound

https://huagongshe.com/reaction/1607842

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 byS. B. Hyeon, I. Nagai, H. Tesaka, 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 byE. 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 residueis 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 byrotary evaporator to give the product, N-[4-(1-hydroxyiminoethyl)phenyl]-N'-allyl-N'-ethoxycarbonylmethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868061
Source datasetuspto-grants-1989_09
ORD IDord-a1783882885d494fa158f1b827db64e3
Source noteuspto-grants-1989_09