HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838615Generated: November 4, 2026
Methanol → 2-Chloro-4,6-dimethoxy-1,3,5-triazine
https://huagongshe.com/reaction/1838615
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Product | 2-Chloro-4,6-dimethoxy-1,3,5-triazine | HCID 18450 | 88.4% |
Reaction Steps
In a 500-ml four-necked flask equipped with a stirrer and a thermometer, 52.6 g (0.525 mol) of potassium hydrogencarbonate and 160.2 g (water content: 340 ppm, 5.0 mol) of methanol were placed. With stirring at a temperature of not higher than 10° C., 46.1 g (0.25 mol) of cyanuric chloride was added, followed by stirring at 20° C. for 1 hour. Then, the reaction was conducted at 50° C. for 2.5 hours. The weight of the reaction solution from which a salt formed had been removed was 193 g, and the water content was 49,600 ppm. After cooling, methanol was distilled off. To the residue, 200 ml of water was added, and the objective product was extracted with 250 ml of ethyl acetate. The organic layer was washed with 100 ml of water and then vacuum concentrated to obtain 38.8 g of 2-chloro-4,6-dimethoxy-1,3,5-triazine as a white solid. The yield was 88.3%. From the gas chromatography analysis, the purity proved to be 96.0% (% by area).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673922B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-3c5ff3a7000b40549cab410e27670b9c |
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| Source note | uspto-grants-2004_01 |
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