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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190281Generated: October 30, 2026

Water → Methyl 2,3,4-trimethoxybenzoate

https://huagongshe.com/reaction/2190281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant2,3,4-Trimethoxybenzoic acidHCID 11308—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2,3,4-trimethoxybenzoateHCID 13940801—

Reaction Conditions

Temperature50 °C

Reaction Steps

2,3,4-Trimethoxybenzoic acid (Aldrich) (20 g, 94 mmol) was dissolved in dry DMF (250 mL). K2CO3 (13 g, 94 mmol) and MeI (6.5 mL, 103.4 mmol) were added and the reaction mixture was heated to 50° C. for 5 h. The reaction mixture was cooled tort and water (250 mL) was added. EtOAc (1 L) was added and the organic phase was washed with water (3×500 mL) and finally with NaCl (sat.). The organic phase washed dried over MgSO4, filtered and concentrated in vacuo. Redissolved in toluene and evaporated. Methyl 2,3,4-trimethoxybenzoate was obtained as a slightly yellow oil. 1H NMR (CDCl3) δ=7.60 (1H, d), 6.70 (1H, d), 3.99 (3H, s), 3.91 (3H, s), 3.89 (3H, s), 3.88 (3H, s). Yield 21 g (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324394B2
Source datasetuspto-grants-2012_12
ORD IDord-448f6cfe3dc3430090206f5fee473c26
Source noteuspto-grants-2012_12