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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280851Generated: November 2, 2026

Dimethylformamide → 6-Methyl-2-nitrobenzoic acid

https://huagongshe.com/reaction/2280851

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 numberUS09139555B2
Source datasetuspto-grants-2015_09
ORD IDord-2b1690f7bc334f118a72278fe2ef2ae6
Source noteuspto-grants-2015_09