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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052104Generated: November 1, 2026

Ethylamine → Atrazine

https://huagongshe.com/reaction/2052104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantSodium HydroxideHCID 14798—
Reactant1,3,5-Triazin-2-amine, 4,6-dichloro-N-(1-methylethyl)-HCID 19453—
SolventTolueneHCID 1140—
ProductAtrazineHCID 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 orde of 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182874
Source datasetuspto-grants-1980_01
ORD IDord-65238ece68054bcaae5c50dac689ef61
Source noteuspto-grants-1980_01