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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653002Generated: October 29, 2026

Methyl Ethyl Ketone → HCID 13532883, compound

https://huagongshe.com/reaction/653002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantHCID 20195211HCID 20195211—
SolventWaterHCID 962—
ProductHCID 13532883HCID 13532883—

Reaction Steps

A mixture of 4-[N-(6-chloro-2-quinazolinyl)-N-methylamino]phenol (0.52 g), ethyl 2-bromopropionate (0.40 g), potassium carbonate (0.28 g) and methyl ethyl ketone (25 ml) was heated under reflux for a period of 18 hours. After cooling, the mixture was diluted with water and the aqueous mixture was extracted with dichloromethane. The dichloromethane extract was dried (anhydrous sodium sulfate) and the solvent was removed under reduced pressure. The residue was purified by chromatography over silica gel (eluant dichloromethane) to give ethyl 2-{4-[N-(6-chloro-2-quinazolinyl)-N-methylamino]phenoxy}propionate as a yellow oil. The assigned structure was confirmed by proton magnetic resonance (pmr) spectroscopy and mass spectrometry. Pmr spectrum (CDCl3 ; δ in ppm): 8.93 (1H, s, quinazoline hetero ring proton); 7.60 (3H, s, quinazoline benzo-ring protons); 7.13 (4H, d of d, phenoxy protons); 4.80 (1H, q, CH--CH3); 4.27 (2H, q, CH2 --CH3); 1.60 (3H, d, CH--CH3); 1.27 (3H, t, CH2 --cH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675047
Source datasetuspto-grants-1987_06
ORD IDord-34742fd74a214b54b59c83d46b9c2a4f
Source noteuspto-grants-1987_06