HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(3,4-Dichlorophenyl)-1-phenoxycarbonyloxy-3-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Urea, N-(3,4-dichlorophenyl)-N-hydroxy-N'-methyl- | HCID 80430 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(3,4-Dichlorophenyl)-1-phenoxycarbonyloxy-3-methylurea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03948967 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-6613350084394748ae63f3fb0dbd3bf9 |
| Source note | uspto-grants-1976_04 |