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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862893Generated: October 31, 2026

Ethylamine → Atrazine

https://huagongshe.com/reaction/1862893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantIsopropylamineHCID 6363—
ReactantCyanuric chlorideHCID 7954—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductAtrazineHCID 2256—

Reaction Conditions

Temperature35 °C

Reaction Steps

Using the apparatus and general procedure described in Illustrative Embodiment IA, a 30.5% by weight solution of cyanuric chloride in acetone was charged to a batch reaction vessel. A less than stoichiometric amount of isopropylamine (the molar ratio of cyanuric chloride to isopropylamine was 1.04) was charged over a period of one hour and then sufficient 20% by weight sodium hydroxide in water was added over a period of 40 minutes to bring the pH of the aqueous phase to 8.0. The temperature of the reaction mixture during both reaction steps was controlled at 10° C. Hydrolysis of the excess cyanuric chloride was effected by reducing the pH to 6.0 and heating the reaction mixture to 35° C. for a period of 0.5 hours. Aqueous sodium hydroxide solution was added as necessary to maintain the pH of the reaction mixture at 6.0. At the conclusion of this reaction step, the pH was increased to 8.0 and ethylamine as a 68% solution in water was added over a period of 30 minutes. Sufficient 20% by weight sodium hydroxide solution was added over a period of 45 minutes to produce a pH of 8.5. The temperature of the reaction mixture was maintained at 35° C. during this reaction sequence. Crude atrazine was isolated from the reaction mixture by precipitation with water. The molar yield of atrazine was 94.3% based on isopropylamine charged to the reaction. The composition of the crude atrazine was determined by gas-liquid chromatography and is given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166909
Source datasetuspto-grants-1979_09
ORD IDord-315ae2488a1a4113bcf2b0ecef92885d
Source noteuspto-grants-1979_09