HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296976Generated: November 4, 2026
Water → 4-(3-bromobenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one
https://huagongshe.com/reaction/2296976
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromobenzyl bromide | HCID 69979 | — |
| Reactant | 3H-1,2,4-Triazol-3-one, 1,2-dihydro-5-methoxy- | HCID 135499741 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(3-bromobenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 18388868 | 29.9% |
Reaction Steps
To a solution of 2.30 g (20 mmol) of 5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one in 20 ml acetonitrile was added 2.90 g (21 mmol) of potassium carbonate. A solution of 5.00 g (20 mmol) of 3-bromobenzylbromide in 20 ml of dry acetonitrile was added dropwise thereto at 55° C. After the mixture was stirred at the same temperature for additional 6 hours, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried and concentrated. To the resultant solid residue (5.2 g) was added a mixture of equal amounts of tert-butyl methyl ether and n-hexane and the solid was washed, ice-cooled, collected by filtration and concentrated. Further, to the resultant solid residue was added tert-butyl methyl ether and the solid was washed, cooled, collected by filtration and dried to obtain 1.70 g (5.98 mmol) of 4-(3-bromobenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489487B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-f8236be7116c468bbe93edc59af9d5e2 |
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| Source note | uspto-grants-2002_12 |
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