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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456029Generated: October 25, 2026

Water → Methyl 2,3,4-trimethoxybenzoate

https://huagongshe.com/reaction/456029

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 to it 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 numberUS08497380B2
Source datasetuspto-grants-2013_07
ORD IDord-3216ad2980eb4cd08a2d71088f0d0ca0
Source noteuspto-grants-2013_07