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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571244Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-(5-hydroxy-6-nitro-1,3-dioxoisoindolin-2-yl)acetate

https://huagongshe.com/reaction/571244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantPotassium nitriteHCID 516910—
ReactantMethyl 2-(5,6-dichloro-1,3-dioxoisoindolin-2-yl)acetateHCID 3710015—
ProductMethyl 2-(5-hydroxy-6-nitro-1,3-dioxoisoindolin-2-yl)acetateHCID 15932847—

Reaction Steps

A mixture of methyl 2-(5,6-dichloro-1,3-dioxoisoindolin-2-yl)acetate (1.420 g, 4.927 mmol) and potassium nitrite (1.678 g, 19.72 mmol) in dry DMF (23 ml) was heated to reflux for 5 hours. The reaction was cooled to room temperature, poured into 0.5N HCl (100 ml) and extracted twice with diethyl ether (2×100 ml). The combined organic layers were washed with 0.5N HCl (120 ml), with brine (100 ml) and dried over sodium sulfate. The solvent was removed, and the crude was purified by chromatography on silica gel cartridge (petroleum ether:ethyl acetate from 90:10 to 100% ethyl acetate). Two different impure fractions of desired compound were isolated. The first fraction was purified by trituration with MeOH affording 0.250 g of title compound. The second fraction was purified by flash chromatography on silica gel cartridge (petroleum ether:ethyl acetate:TFA from 80:20:0.2 to ethyl acetate:TFA=100:0.2) to obtain 0.160 g of title compound. The two clean portions of desired compound were mixed affording methyl 2-(5-hydroxy-6-nitro-1,3-dioxoisoindolin-2-yl)acetate (0.410 g, 1.463 mmol, 30% yield). MS/ESI+ 281.1 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-79e48c8dfb0b42f686aa6bf7b6ab8259
Source noteuspto-grants-2015_05