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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584236Generated: October 30, 2026

2-Bromoethanol → HCID 22342574, compound

https://huagongshe.com/reaction/584236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Oxa-4-azaspiro[2.5]octane hydrochlorideHCID 22342972—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 22342574HCID 22342574—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 7-oxa-4-azaspiro[2.5]octane hydrochloride (200 mg), 2-bromoethanol (0.28 ml) and potassium carbonate (550 mg) in N,N-dimethylformamide (2 ml) was stirred at 90° C. for 48 hours and cooled. The mixture was poured into brine and extracted with dichloromethane. The extract was dried over magnesium sulfate and evaporated under reduced pressure, and purified by column chromatography on silica gel using a mixture of methanol and chloroform (2:98) to give 4-(2-hydroxyethyl)-7-oxa-4-azaspiro[2.5]octane as an oil. This oil was dissolved in ethyl acetate (5 ml) and the solution was added methanesulfonyl chloride (0.16 ml) and triethylamine (0.3 ml). After 30 minutes of stirring at room temperature, the mixture was filtered, evaporated, and purified by column chromatography on silica gel using a mixture of ethyl acetate and n-hexane (20:80˜30:70) to give 4-(2-chloroethyl)-7-oxa-4-azaspiro[2.5]octane (140 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-ccdfaf1d84b4455c9ca95872628ec6fb
Source noteuspto-grants-2005_08