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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686085Generated: October 26, 2026

Water → Methyl 2,3,4-trimethoxybenzoate

https://huagongshe.com/reaction/1686085

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 rt 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 numberUS08148537B2
Source datasetuspto-grants-2012_04
ORD IDord-f64a66f2df9c42448b36e8dfe1429527
Source noteuspto-grants-2012_04