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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575019Generated: October 29, 2026

Potassium Carbonate → Butanoic acid, 4-(4-bromo-3-fluorophenoxy)-, ethyl ester

https://huagongshe.com/reaction/575019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant4-Bromo-3-fluorophenolHCID 2779153—
CatalystSodium IodideHCID 5238—
SolventAcetoneHCID 180—
ProductButanoic acid, 4-(4-bromo-3-fluorophenoxy)-, ethyl esterHCID 86693053100.9%

Reaction Conditions

Temperature56 °C

Reaction Steps

Into a 2000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of argon was placed 4-bromo-3-fluorophenol (50 g, 261.78 mmol, 1.00 equiv), acetone (500 mL), NaI (2.8 g, 0.07 equiv), potassium carbonate (54.2 g, 392.16 mmol, 1.50 equiv), and ethyl 4-bromobutanoate (61.3 g, 314.27 mmol, 1.20 equiv). The resulting solution was stirred at 56° C. overnight. The solids were filtered out and the filtrate was concentrated under vacuum. The residue was dissolved in 1000 mL of EA and the resulting mixture was washed with 2×100 mL of sodium hydroxide (1 N) and 3×100 mL, of water. The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum to afford 80.6 g (crude) of ethyl 4-(4-bromo-3-fluorophenoxy)butanoate as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-361afcae56044c0aa5c0f8073870e614
Source noteuspto-grants-2015_05