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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660129Generated: October 29, 2026

Benzyl bromoacetate → HCID 20557555, compound

https://huagongshe.com/reaction/1660129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl bromoacetateHCID 62576—
ReactantHCID 20557501HCID 20557501—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 20557555HCID 2055755552.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307094
Source datasetuspto-grants-1981_12
ORD IDord-cfef32a872624689b3b5b231855fef83
Source noteuspto-grants-1981_12