HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453645Generated: October 30, 2026
Methanol → 2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dione
https://huagongshe.com/reaction/453645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | 1,2,4-Triazine, 3,5-bis[(trimethylsilyl)oxy]- | HCID 87057 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dione | HCID 15817175 | 76.5% |
Reaction Steps
22.1 g of 3,5-Bis-trimethylsilanyloxy-[1,2,4]triazine (86 mmol) were dissolved in 150 mL of dichloroethane followed by addition of 14.7 g of 1-bromo-4-chloro-butane (86 mmol) and 0.218 g of iodine (0.858 mmol). The reaction mixture was stirred for 25 h at room temperature. Then, 300 mL of methanol were added and the mixture was stirred for an additional 10 minutes. The solvents were evaporated under reduced pressure and the residue was partitioned between dichloromethane and water. The aqueous phase was extracted several times with dichloromethane. The combined organic layers were washed with 10% aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and the organic phase was evaporated under reduced pressure. The thus obtained crude product was purified via silica gel chromatography using dichloromethane-methanol 0-10% to yield 13.4 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492540B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-53ded76454e04703a7aef4522fde93ca |
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| Source note | uspto-grants-2013_07 |
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