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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708795Generated: October 29, 2026

Methanol → Methyl 2-methyl-4-nitrobenzoate

https://huagongshe.com/reaction/708795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Nitro-o-toluic acidHCID 74790—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-methyl-4-nitrobenzoateHCID 15088700100%

Reaction Conditions

Temperature40 °C

Reaction Steps

To 2-methyl-4-nitrobenzoic acid (10.5 g, 58.0 mmol) in CH2Cl2 (80 ml) was added 2.0 M oxalyl chloride in methylene chloride (39.9 ml, 80 mmol), followed by DMF (0.224 ml, 2.90 mmol). The mixture was stirred at 40° C. for 1.5 h and then at rt for 0.5 h. Solvent was removed and the residue was put on high vacuum for 0.5 h. The acyl chloride prepared was then dissolved in methylene chloride (40 mL) and cooled at 0° C., MeOH (40 mL) was added and the mixture was stirred at 0° C. for 0.5 h. Solvent was removed, the crude was diluted with EtOAc, washed with sat. sodium bicarbonate, brine. The organic layer was dried over sodium sulfate and concentrated to give Intermediate 3A (11.35 g, 58.2 mmol, 100% yield) as a white solid. 1H NMR (400 MHz, chloroform-d) δ ppm 7.98-8.11 (m, 3H) 3.93 (s, 3H) 2.67 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174974B2
Source datasetuspto-grants-2015_11
ORD IDord-472913938d6f419297eceeb05d1c306b
Source noteuspto-grants-2015_11