HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755700Generated: October 30, 2026
Hydrochloric Acid → 2,4-Dichloro-6-phenyl-1,3,5-triazine
https://huagongshe.com/reaction/1755700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dichloro-6-phenyl-1,3,5-triazine | HCID 15549 | 61% |
Reaction Steps
7.80 g (0.32 mol) of iodine-activated magnesium turnings in 20 ml of anhydrous THF are heated briefly to 60° C. Then 47.1 g (0.30 mol) of bromobenzene and 80 ml of THF are added dropwise over 30 min and the mixture is heated for 1.5 hours to 65° C. After cooling, the Grignard solution is added over 1 hour to a mixture of 51.6 g (0.28 mol) of cyanuric chloride and 140 ml of THF, while keeping the temperature of the mixture in the range from 10° to 20° C. When the addition is complete, the mixture is stirred at for 3 hours at 25° C. The mixture is then diluted with 280 ml of toluene, the resultant suspension is poured into 300 g of 12% aqueous HCl, the organic phase is separated, washed with a total amount of 400 g of water and concentrated. The resultant material (melting point 117°-120° C.) is recrystallised from hexane, giving the title compound in a yield of 61%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05438138 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-d4b762a83d774b57ad5c874b61977fa7 |
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| Source note | uspto-grants-1995_08 |
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