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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803024Generated: November 2, 2026

Dimethylformamide → 4-((3,5,6-Trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid ethyl ester

https://huagongshe.com/reaction/1803024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl syringateHCID 19845—
Reactant2-(Bromomethyl)-3,5,6-trimethylpyrazineHCID 13584992—
SolventWaterHCID 962—
Product4-((3,5,6-Trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid ethyl esterHCID 5947992261.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

Adding 2-bromomethyl-3,5,6-trimethylpyrazine (0.44 g, 0.002 mol), syringic acid ethyl ester (0.54 g, 0.0024 mol), anhydrous potassium carbonate (0.72 g, 0.005 mol), and DMF (20 mL) into a 100 mL three-necked bottle in turn, wherein the solution appears orange and turbid, irradiating with incandescent lamp, heating to 90° C., stifling to react for 12 hours, TLC [V(petroleum ether):V(ethyl acetate)=3:1 as developing agent] detecting shows that reaction is complete, (Rf of raw material=0.7, Rf of product=0.5), and the reaction solution appears deep yellow, filtering to obtain orange filtrate, adding 30 mL water, extracting with chloroform (3×30 mL), incorporating the chloroform layer and wishing with water (2×20 mL), drying with anhydrous sodium sulfate, recycling chloroform under reduced pressure to obtain a light yellow oily matter, separating with a silica column, wherein eluant is V(cyclohexane):V(ethyl acetate)=3:1, collecting product, recycling the solution under reduced pressure to obtain 0.45 g light yellow 4-((3,5,6-trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid ethyl ester, a yield is 61.6%, m.p. 121.7-123.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350033B2
Source datasetuspto-grants-2013_01
ORD IDord-9b187ff8fe8c483d8cefdec6f4fb0ed0
Source noteuspto-grants-2013_01