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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370510Generated: November 3, 2026

3,5-Dinitrobenzoic acid → Methyl 3,5-dinitrobenzoate

https://huagongshe.com/reaction/1370510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dinitrobenzoic acidHCID 7433—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ProductMethyl 3,5-dinitrobenzoateHCID 22206797.3%

Reaction Steps

To 3,5-Dinitro-benzoic Acid (Aldrich, 21.2 g, 100 mmol) was added SOCl2. The mixture was refluxed overnight. The excess SOCl2 was removed under reduced pressure. The residue was dissolved in 100 mL of MeOH, cooled in ice bath, and triethylamine (Aldrich, 21 mL, 150 mmol) was added slowly added. After the mixture was stirred at ambient temperature for 3 h, solvent was removed under reduced pressure. The residue was diluted with EtOAc and 1N HCl. The mixture was extracted 3× with EtOAc (100 mL). The organic layers were washed twice with a brine solution (100 mL), dried over Na2SO4. Removal of the solvent gave 22.0 g (97%) of product, which was pure enough for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583157B2
Source datasetuspto-grants-2003_06
ORD IDord-f3427f9e172d4594a7ef67c675057c18
Source noteuspto-grants-2003_06