Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 4,6-dichloro-N-phenyl-1,3,5-triazin-2-amine | HCID 16766 | — |
| Product | HCID 21558484 | HCID 21558484 | — |
Reaction Steps
A solution of 30 parts of dichlorosulphonylisocyanate in 100 parts of dry acetronitrile is slowly added dropwise to a suspension of 48.22 parts of 2,4-dichloro-6-phenylamino-s-triazine in 100 parts by volume of dry acetonitrile. The mixture is warmed gently and soon a clear, slightly yellowish solution forms. The reaction is brought to completion by subsequently stirring the solution for about 2 hours at 45°-50°C and then for 2 hours at room temperature. Then 320 parts by volume of water are added in such a manner that the temperature rises initially to 70°-75°C but is then immediately lowered. The precipitate which has formed is filtered off with suction, washed neutral with water and dried in vacuo to yield 52 parts of N-(2,4-dichloro-s-triazin-6-yl)-N-phenyl-urea which melts at 151°-154°C and is pure enough for most reactions. Recrystallisation from perchloroethylene yields a white, crystalline product which melts at 155°-157°C and has the following analytical values:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03939158 |
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| Source dataset | uspto-grants-1976_02 |
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| ORD ID | ord-aeacdf33bd654300b5fb4c32dc71d170 |
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| Source note | uspto-grants-1976_02 |
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