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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260803Generated: October 31, 2026

Sulfuric Acid → 3-Methoxy-2-MethylBenzoic Acid

https://huagongshe.com/reaction/260803

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 Conditions

Temperature55 °C

Reaction Steps

3-Amino-2-methylbenzoic acid, 140.3 grams (g), 0.93 mole, reacted in four portions) in 5.7 mass equivalents of methanol, was treated with 1.5 mole equivalents of concentrated sulfuric acid. The mixture was heated to 55° C. and 1.05 mole equivalent of sodium nitrite dissolved in twice its mass of water was fed to the reaction over 30 to 45 minutes, maintaining the temperature between 55° and 65° C. Then 4.5 mole equivalents of 25% aqueous sodium hydroxide was added over one-half hour, followed by a half-hour feed of 2 mole equivalents of dimethyl sulfate at 50° to 60° C. After one-half hour the batch was assayed by gas chromatography (GC). Additional sodium hydroxide and dimethyl sulfate were added in portions until complete conversion was obtained, The methanol remaining was removed by vacuum, and the residue was partitioned between ethyl acetate and water made acidic with sulfuric acid. The ethyl acetate was removed under vacuum. The combined residues (152.8 g) dissolved in 350 g warm methanol were poured into a mixture of 278 g concentrated sulfuric acid and 1 liter (L) water. The resulting precipitate was collected by filtration, washed with water, and dried in vacuo, giving 135.8 g of material which was 96% pure as determined by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05530028
Source datasetuspto-grants-1996_06
ORD IDord-5b811557972e4daeaff60246a366d139
Source noteuspto-grants-1996_06