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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803025Generated: November 1, 2026

Sodium Hydroxide → 4-((3,5,6-Trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid

https://huagongshe.com/reaction/1803025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-((3,5,6-Trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid ethyl esterHCID 59479922—
SolventWaterHCID 962—
Product4-((3,5,6-Trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acidHCID 5947992195.4%

Reaction Steps

Adding water (20 mL), NaOH (0.14 g, 3.5 mmol) into a 100 mL round-bottom flask, stirring to dissolve, then adding 95% alcohol (20 mL), 4-((3,5,6-trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid ethyl ester (1.00 g, 2.8 mmol), stifling under room temperature to react for 4 hours, TLC [V(petroleum ether):V(ethyl acetate)=3:1 as developing agent] detecting shows that reaction is complete, (Rf of raw material=0.5, Rf of product=0), distilling out the alcohol under reduced pressure, adjusting pH of the reaction solution to 4-5 with 1.0M HCl while keeping the reaction solution cool to separate out solid, filtering, washing the solid with cool water for three times, processing with vacuum filtration, recrystallizing with anhydrous alcohol, drying under 70° C. for 8 hours to obtain 0.88 g white crystalloid of 4-((3,5,6-trimethylpyrazine-2-yl)methoxyl)-3,5-dimethoxybenzoic acid, wherein a yield is 95.4%, m.p.>218° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350033B2
Source datasetuspto-grants-2013_01
ORD IDord-9900bc4073c44ae2a5bfc221b62585aa
Source noteuspto-grants-2013_01