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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dichloro-6-cyclopropyl-1,3,5-triazine | HCID 18965220 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Chloro-4-cyclopropyl-6-morpholino-1,3,5-triazine | HCID 18965207 | 76.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258513 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-3cfee7b7e7a1454599bd237dd79c0e39 |
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| Source note | uspto-grants-1993_11 |
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