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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403985Generated: October 25, 2026

Nitric Acid → Ethyl 5-methyl-2,4-dinitrobenzoate

https://huagongshe.com/reaction/1403985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant3-Methylbenzoic acidHCID 7418—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Methyl-2,4-dinitrobenzoic acidHCID 3671900—
Reactant3-Methyl-2,6-dinitrobenzoic acidHCID 54096940—
SolventEthanolHCID 702—
ProductEthyl 5-methyl-2,4-dinitrobenzoateHCID 1518463225.4%

Reaction Steps

To a mixture of HNO3 (95%, 80 mL) and H2SO4 (98%, 80 mL) was slowly added 3-methylbenzoic acid (50 g, 0.37 mol) at 0° C. After addition, the mixture was stirred below 30° C. for 1.5 hours. The mixture was then poured into ice-water and stirred for 15 min. The precipitate solid was filtered and washed with water to give a mixture of 3-methyl-2,6-dinitro-benzoic acid and 5-methyl-2,4-dinitrobenzoic acid (70 g, 84%). To a solution of this mixture (70 g, 0.31 mol) in EtOH (150 mL) was added dropwise SOCl2 (54 g, 0.45 mol). The mixture was heated at reflux for 2 h before being concentrated to dryness under reduced pressure. The residue was partitioned between EtOAc (100 mL) and aq. Na2CO3 (10%, 120 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4, and concentrated to dryness to obtain ethyl 5-methyl-2,4-dinitrobenzoate (20 g), which was placed aside. The aqueous layer was acidified by HCl to pH 2˜3 and the precipitated solid was filtered, washed with water, and dried in air to give 3-methyl-2,6-dinitrobenzoic acid (39 g, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912199B2
Source datasetuspto-grants-2014_12
ORD IDord-39e4641fe9564ff580f0f66ce482a498
Source noteuspto-grants-2014_12