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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892132Generated: October 29, 2026

Ethyl Acetate → Methyl 2-methyl-6-[3-(quinolin-2-ylmethoxy)-phenoxymethyl]-benzoate

https://huagongshe.com/reaction/892132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(bromomethyl)-6-methylbenzoateHCID 10263795—
ReactantPhenol, 3-(2-quinolinylmethoxy)-HCID 10988736—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-methyl-6-[3-(quinolin-2-ylmethoxy)-phenoxymethyl]-benzoateHCID 22241476—

Reaction Conditions

Temperature85 °C

Reaction Steps

13-(Quinolin-2-ylmethoxy)-phenol (5.2 g, 21 mmol, example 3), methyl 2-bromomethyl-6-methyl-benzoate (example 2) (5.0 g, 21 mmol) and potassium carbonate (4.4 g, 32 mmol) are combined in DMF (50 mL) and heated at 85° C. for 3 h. The reaction is poured into ethyl acetate (500 mL) and washed with water (4×120 mL) and brine (100 mL). The solution is dried over magnesium sulfate, filtered and concentrated in vacuo to provide a residue which is purified by column chromatography (silica, 10 to 20% ethyl acetate in hexane) to provide the title compound. MS (ESI) 414 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005440B1
Source datasetuspto-grants-2006_02
ORD IDord-cf1ccdfa8c5c4910b8291994e1d57646
Source noteuspto-grants-2006_02