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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605076Generated: October 31, 2026

Triethylamine → 1-(3,4-Dichlorophenyl)-1-phenoxycarbonyloxy-3-methylurea

https://huagongshe.com/reaction/1605076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
ReactantUrea, N-(3,4-dichlorophenyl)-N-hydroxy-N'-methyl-HCID 80430—
SolventDiethyl EtherHCID 3283—
Product1-(3,4-Dichlorophenyl)-1-phenoxycarbonyloxy-3-methylureaHCID 21549086—

Reaction Steps

A solution of 1-(3,4-dichlorophenyl)-1-hydroxy-3-methylurea (6 grams; 0.025 mol) in diethyl ether (200 ml), and triethylamine (4 ml) were charged into a glass reaction flask equipped with a mechanical stirrer. Phenyl chloroformate (4.2 grams; 0.027 mol) was added thereto. The reaction mixture was stirred, at room temperature, for a period of about one-half hour resulting in the formation of a precipitate. The precipitate was recovered by filtration, was washed with water, dried, and was recrystallized from a methylene chloride-pentane mixture to yield 1-(3,4-dichlorophenyl)-1-phenoxycarbonyloxy-3-methylurea melting at 93°C with decomposition and having the following elemental analysis as calculated for C15H12Cl2N2O4 :

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03948967
Source datasetuspto-grants-1976_04
ORD IDord-6613350084394748ae63f3fb0dbd3bf9
Source noteuspto-grants-1976_04