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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525901Generated: November 1, 2026

Potassium Carbonate → Methyl 2-(4-bromo-2-fluorophenyl)-2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)acetate

https://huagongshe.com/reaction/1525901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-bromo-2-(4-bromo-2-fluorophenyl)acetateHCID 53429414—
ReactantHCID 69083351HCID 69083351—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-bromo-2-fluorophenyl)-2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)acetateHCID 7127094491.9%

Reaction Steps

A solution of methyl 2-bromo-2-(4-bromo-2-fluorophenyl)acetate (7.29 mmol) in N,N-dimethylformamide (30 mL) was treated with potassium carbonate (19.90 mmol) and 4-cyclopropyl-1-oxa-4,9-diazaspiro[5.5]undecan-3-one hydrochloride (8.31 mmol). The reaction was stirred at room temperature for two days. The reaction solution was diluted with water (200 mL) and was extracted three times with ethyl acetate. The combined organic layers were washed five times with water and three times with brine. The organic solution was dried over sodium sulfate, filtered and concentrated in vacuo. The resulting semi-solid was diluted with dichloromethane (10 mL) and was concentrated to dryness in vacuo. This was repeated twice, at which point the resulting solid was dried under high vacuum overnight, affording the title compound as a white solid (3.05 g, 87% yield). MS(ES)+ m/e 454.8/456.9 [M+H]+ (bromide isotope pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09084794B2
Source datasetuspto-grants-2015_07
ORD IDord-095f29ec5e804714b77fd2fd13ec755e
Source noteuspto-grants-2015_07