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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260805Generated: October 31, 2026

Sulfuric Acid → 3-Methoxy-2-MethylBenzoic Acid

https://huagongshe.com/reaction/260805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactant3-Amino-2-methylbenzoic acidHCID 2733699—
ReactantSodium NitriteHCID 23668193—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Methoxy-2-MethylBenzoic AcidHCID 7021483—

Reaction Steps

Ground 3-amino-2-methylbenzoic acid (17 g, 0.11 mole) was mixed with methanol (120 mL) in a 1-13-neck round bottom flask provided with a mechanical stirrer and a thermometer. To this mixture, concentrated sulfuric acid, 15.5 mL, was added dropwise with stirring. Upon the addition, the temperature of the mixture went up to 50° C. The addition time was 2 minutes. Following the addition, the flask was placed on a pre-heated oil bath and the temperature of 50°-55° C. inside the flask was maintained. Thereafter, a dropwise addition of sodium nitrite solution (8.1 g in 17 mL of water) was started. When the temperature reached 62° C., the heating under the oil bath was turned off. After additional 10 min on the oil bath (the heater still turned off), the temperature dropped to 55° C., at which point sodium hydroxide (50% aqueous, 55 g) diluted water (55 mL) was added dropwise over 30 minutes, followed by water (55 mL) in one portion, and dimethyl sulfate (25 mL) dropwise in two portions (15 mL plus 10 mL) over 30 minutes with 20 minutes apart. The reaction mixture was allowed to cool to room temperature whereupon it was poured over concentrated sulfuric acid, 40 mL, diluted with water (360 mL), the product collected by filtration, and dried in vacuo over 24 hours to give 3-methoxy-2-methylbenzoic acid (12 g). 1H-NMR (CDCl3) δppm 2.50 (s, 3H), 3.85 (s, 3H), 7.03 (d 1H, Ar), 7.22 (dd, 1H, C-5), 7.59 (d, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05530028
Source datasetuspto-grants-1996_06
ORD IDord-6b4717947e13434f97245d646a45e287
Source noteuspto-grants-1996_06