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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023972Generated: October 30, 2026

Sodium Iodide → 4-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenoxy]-butyric acid ethyl ester

https://huagongshe.com/reaction/1023972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantTetrabutylammoniumHCID 16028—
ReactantAmmonium ChlorideHCID 25517—
ReactantButanoic acid, 2-bromo-, ethyl esterHCID 79039—
Reactant4-[2-(Benzyloxy)-4-ethylphenoxy]-3-fluorophenolHCID 59191235—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product4-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenoxy]-butyric acid ethyl esterHCID 5919136575%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluorophenol (0.30 mmol; 100 mg) in dry acetone (2 mL), under argon, were added potassium carbonate (0.35 mmol; 49 mg), NaI (0.06 mmol; 9 mg) and ethyl bromobutyrate (0.35 mmol; 51 μL). The reaction was stirred 14 hours at 60° C. Water (100 μL) and tetrabutylammonium hydroxyde (0.03 mmol; 8 mg) were added and the mixture was stirred 16 hours at 60° C. The reaction was hydrolysed with NH4Cl sat. (5 mL) and extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (100 mg; 0.22 mmol; 75%) was obtained as a yellow oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722746B2
Source datasetuspto-grants-2014_05
ORD IDord-97b5beb9de2e4f01b6c943fdefa26c35
Source noteuspto-grants-2014_05