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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713560Generated: November 2, 2026

Ethyl bromoacetate → HCID 86761174, compound

https://huagongshe.com/reaction/1713560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 23121958HCID 23121958—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86761174HCID 8676117490.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of hexahydro-1,1-diphenyl-7-[(4-piperidinyl)carbonyl]-3H-oxazolo[3,4-a]pyrazin-3-one hydrochloride (0.20 g, 0.45 mmol) and potassium carbonate (0.16 g, 1.2 mmol) in tetrahydrofuran (5 mL) was added ethyl bromoacetate (0.055 mL, 0.50 mmol) at 0° C., and the mixture was stirred at 0° C. for 2 hours and at room temperature for 20 hours. The reaction solution was diluted with water and then extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over magnesium sulfate. The solid was filtered off, and the filtrate was concentrated and dried to a solid. The residue was purified with silica gel column chromatography (ethyl acetate to ethyl acetate:methanol=9:1) to obtain the title compound (0.20 g, yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795267B2
Source datasetuspto-grants-2010_09
ORD IDord-f5e9be64c1374ad38327d3e51b560bcc
Source noteuspto-grants-2010_09