HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660129Generated: October 29, 2026
Benzyl bromoacetate → HCID 20557555, compound
https://huagongshe.com/reaction/1660129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | HCID 20557501 | HCID 20557501 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 20557555 | HCID 20557555 | 52.2% |
Reaction Steps
1.50 g (0.007 mol) of methyl hexahydro-1,3-dioxo-1H-1,2,4-triazolo[1,2-a]pyridazine-5-carboxylate were dissolved in 40 ml of dry tert.butanol. A solution of 0.87 g (0.008 mol) of potassium tert.butoxide in 50 ml of dry tert.butanol was added and the mixture was stirred under reflux and under a nitrogen atmosphere for 4 hours. 1.61 g (0.007 mol) of benzyl bromoacetate were added and the heating was continued for a further 4 hours. The mixture was filtered and the filtrate was evaporated to dryness. The residue was chromatographed on silica gel using chloroform for the elution to give 1.32 g (52%) of benzyl 5-methoxycarbonyl-2,3,5,6,7,8-hexahydro-1,3-dioxo-1H-1,2,4-triazolo[1,2-a]pyridazine-2-acetate of melting point 103°-106° C. (from dichloromethane/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04307094 |
|---|
| Source dataset | uspto-grants-1981_12 |
|---|
| ORD ID | ord-cfef32a872624689b3b5b231855fef83 |
|---|
| Source note | uspto-grants-1981_12 |
|---|