Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(1-methylethyl)- | HCID 19453 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Atrazine | HCID 2256 | — |
Reaction Steps
To the solution of 2,4-dichloro-6-isopropylamino-s-triazine in toluene remaining in the reactor are added, under strong agitation, about 915 g of an aqueous solution containing 50% by weight of ethylamine (10.15 moles) and about 1353 g of an aqueous solution containing 30% by weight of sodium hydroxide (10.15 moles). The said solutions are added in the same manner as in the first reaction step. During the second addition the temperature rises from 25° to 50° C. and the final pH is equal to 11-12. The dense suspension thus obtained is divided into two parts as quickly as possible. One part (A) is submitted to distillation to remove the toluene in the form of an azeotropic toluene-water mixture, by operating at 85°-100° C. To the distillation residue are added 3,700 ml of water and the suspension thus obtained is filtered at 60° C. The filtered solid is washed until the sodium chloride has been removed completely. After drying for ten hours in an oven at 100° C., 2-chloro-4-ethylamino-6-isopropylamino-s-triazine is obtained with a yield of the order of 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04230853 |
|---|
| Source dataset | uspto-grants-1980_10 |
|---|
| ORD ID | ord-fddb1ed53e364932ba4a2180ca776e5a |
|---|
| Source note | uspto-grants-1980_10 |
|---|