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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446880Generated: October 25, 2026

Potassium Carbonate → HCID 13314825, compound

https://huagongshe.com/reaction/1446880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant4-[N-Methyl-N-(6-bromo-2-benzoxazolyl)amino]phenolHCID 13314820—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 13314825HCID 1331482553.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-[N-methyl-N-(6-bromo-2-benzoxazolyl)amino]phenol (0.6, 0.002 mole), ethyl 2-bromopropionate (0.4 g, 0.002 mole), anhydrous potassium carbonate (0.3 g, 0.002 mole) and methyl ethyl ketone (6 ml) was heated under reflux, with stirring, for a period of 3 hours. Thin layer chromatography indicated that the reaction had not gone to completion and therefore further anhydrous potassium carbonate (0.15 g) and methyl ethyl ketone was added and the mixture was heated under reflux for a further period of 3 hours. The solvent was removed by distillation under reduced pressure, water (50 ml) was added to the residue and the aqueous mixture was extracted with diethyl ether (3×30 ml). The combined extracts were washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated to give a dark red oil. The oil was heated at a temperature of 100° C. at a pressure of 0.1 mm Hg for a period of 2 hours to remove residual ethyl 2-bromopropionate and the residue was recrystallised from hexane/cyclohexane to give the title compound as a white solid (0.45 g), mp 91°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04314065
Source datasetuspto-grants-1982_02
ORD IDord-bf9ccb253a364288b7ba29f9a3654b5e
Source noteuspto-grants-1982_02