Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Urea, N-(3,4-dichlorophenyl)-N-hydroxy-N'-methyl- | HCID 80430 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21549073 | HCID 21549073 | — |
Reaction Steps
A solution of 1-(3,4-dichlorophenyl)-1-hydroxy-3-methylurea (15 grams; 0.06 mol) is isopropyl alcohol (50 ml), and pyridine (7 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer. Ethyl chloroformate (7 ml; 0.09 mol) was then slowly added, with stirring, at a temperature of 10° to 15°C. After the addition was completed stirring was continued for an additional period of about one-half hour resulting in the formation of a precipitate. After this time, the reaction mixture was poured onto ice and the precipitate recovered by filtration. The precipitate was recrystallized from a benzene-hexane mixture to yield 1-(3,4-dichlorophenyl)-1-ethoxycarbonyloxy-3-methylurea having a melting point of 97°-98°C and having the following elemental analysis as calculated for C11H12Cl2N2O4 :
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03948967 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-cd023419143e47018672df7d0e50cf90 |
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| Source note | uspto-grants-1976_04 |
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