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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011275Generated: November 1, 2026

Dimethylformamide → 6-Methyl-2-nitrobenzoic acid

https://huagongshe.com/reaction/1011275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
ReactantMethyl 2-(bromomethyl)-4-nitrobenzoateHCID 15088701—
Product6-Methyl-2-nitrobenzoic acidHCID 16097—
ProductN-bromobutanimideHCID 67184—
ProductMethyl 2-(bromomethyl)-4-nitrobenzoateHCID 15088701—

Reaction Steps

This compound can be prepared according to the methods described in U.S. Pat. Nos. 6,281,230 and 5,635,517, the entireties of which are incorporated herein by reference. For example, the compound can be prepared through catalytic hydrogenation of 3-(4-nitro-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione. 3-(4-Nitro-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione can be obtained by allowing 2,6-dioxopiperidin-3-ammonium chloride to react with methyl 2-bromomethyl-4-nitrobenzoate in dimethylformamide in the presence of triethylamine. The methyl 2-bromomethyl-4-nitrobenzoate in turn is obtained from the corresponding methyl ester of nitro-ortho-toluic acid by conventional bromination with N-bromosuccinimide under the influence of light.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977357B2
Source datasetuspto-grants-2011_07
ORD IDord-66e3bf9ed82342cc971af9debe2d96b9
Source noteuspto-grants-2011_07