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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781381Generated: November 1, 2026

1,2-Dibromoethane → 5-(2-Bromoethoxy)benzofurazan

https://huagongshe.com/reaction/1781381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
Reactant5-HydroxybenzofurazanHCID 135456836—
SolventEthanolHCID 702—
Product5-(2-Bromoethoxy)benzofurazanHCID 1904535141%

Reaction Steps

Sodium hydroxide (40 mg, 1 mmol) was added to a solution of 5-hydroxybenzofurazan (136 mg, 1 mmol) in ethanol (2 ml) and the mixture was stirred at room temperature for 30 min. 1,2-dibromoethane (0.26 ml, 0.56 g, 3 mmol) was added and the mixture was heated under reflux for 20 hr., cooled and the solvent was evaporated under reduced pressure. Aqueous sodium bicarbonate (saturated, 10 ml) was added and the mixture was extracted with dichloromethane (3×10 ml). The combined organic fractions were dried (Na2SO4) and evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with hexane/10% EtOAc to give the benzofurazan as a pale yellow oil (99 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633247
Source datasetuspto-grants-1997_05
ORD IDord-3a716ce8682049ba850c6a9e0138388f
Source noteuspto-grants-1997_05