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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027248Generated: October 29, 2026

Iodoethane → 2-(3-(Benzyloxy)-4-bromo-5-ethoxyphenyl)-5-methyloxazole

https://huagongshe.com/reaction/1027248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Benzyloxy)-2-bromo-5-(5-methyloxazol-2-yl)phenolHCID 86710655—
SolventDimethylformamideHCID 6228—
SolventDiethylether ethylacetateHCID 21584169—
Product2-(3-(Benzyloxy)-4-bromo-5-ethoxyphenyl)-5-methyloxazoleHCID 8671065695.1%

Reaction Steps

Iodoethane (111 uL, 1.37 mmol) was added to a mixture of 3-(benzyloxy)-2-bromo-5-(5-methyloxazol-2-yl)phenol (412 mg, 1.14 mmol) and potassium carbonate (632 mg, 4.58 mmol) in DMF (2.8 mL). After stirring for two hours, the solution was diluted with 1:1 ethyl acetate/diethyl ether, washed with water (5×), brine, dried over magnesium sulfate and concentrated to provide 2-(3-(benzyloxy)-4-bromo-5-ethoxyphenyl)-5-methyloxazole as a white crystalline solid (421 mg). MS (M+1)=388.2. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.52 (d, J=7.07 Hz, 2H), 7.36-7.43 (m, 2H), 7.28-7.35 (m, 2H), 7.23 (d, J=1.52 Hz, 1H), 6.86 (d, J=1.52 Hz, 1H), 5.24 (s, 2H), 4.21 (q, J=6.74 Hz, 2H), 2.41 (d, J=1.01 Hz, 3H), 1.50 (t, J=6.82 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-f45a5fdfe8aa4c01b71ae63fce4474e8
Source noteuspto-grants-2014_05