HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395621Generated: October 29, 2026
Cyanuric chloride → 2,4-Dichloro-6-morpholino-1,3,5-triazine
https://huagongshe.com/reaction/2395621
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2,4-Dichloro-6-morpholino-1,3,5-triazine | HCID 81076 | 68% |
Reaction Steps
Cyanuric chloride (7.30 g, 39.6 mmol) was dissolved in ethylene glycol dimethyl ether (100 ml), cooled to -15° C. and gradually added dropwise with morpholine (7.00 ml, 80.3 mmol) dissolved in ethylene glycol dimethyl ether (50 ml). This reaction mixture was stirred at the same temperature for 30 minutes and then stirred at room temperature overnight. The reaction mixture was evaporated under reduced pressure. The residue was added with dichloromethane and water, and then shaken for mixing. The organic layer was separated from the mixture, washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the obtained residue was purified by silica gel column chromatography, using n-hexane and ethyl acetate (6:4) as eluant, to obtain 6.32 g (yield: 68.0%) of 2,4-dichloro-6-morpholino-1,3,5-triazine as colorless crystals having melting point of 160.5° C.-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489591 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-24547553f6a648f1b4242ebad1b7d6c9 |
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| Source note | uspto-grants-1996_02 |
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