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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256709Generated: October 25, 2026

Morpholine → 2-Chloro-4-cyclopropyl-6-morpholino-1,3,5-triazine

https://huagongshe.com/reaction/256709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Dichloro-6-cyclopropyl-1,3,5-triazineHCID 18965220—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-Chloro-4-cyclopropyl-6-morpholino-1,3,5-triazineHCID 1896520776.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of 2.61 g (0.03 mole) of morpholine in 20 ml of chloroform is added in the course of 30 minutes to a solution of 5.7 g (0.03 mole) of 2,4-dichloro-6-cyclopropyl-1,3,5-triazine in 50 ml of chloroform, cooled to between 3° and 5° C. The temperature of the mixture is allowed to return to about 10° C., then the mixture is cooled again to 5° C. and a solution of 4.14 g (0.03 mole) of potassium carbonate in 15 ml of water is added dropwise. The mixture is then stirred at room temperature for two hours. 30 ml of water are added and the organic phase is separated off. The solution is washed with water and dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by chromatography on silica (eluent: 96.5:3.5 (v/v) dichloromethane-ethylacetate) and then recrystallized from hexane. 5.5 g of 2-chloro-4-cyclopropyl-6-morpholino-1,3,5-triazine are thus obtained. Yield: 76.2%. M.P.: 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258513
Source datasetuspto-grants-1993_11
ORD IDord-3cfee7b7e7a1454599bd237dd79c0e39
Source noteuspto-grants-1993_11