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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841689Generated: November 1, 2026

Nitric Acid → Methyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1841689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant1-MethylimidazoleHCID 1390—
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant1-MethylpyrroleHCID 7304—
Reactant4-Tert-butoxycarbonylamino-1-methyl-1h-pyrrole-2-carboxylic acid benzotriazol-1yl esterHCID 2755987—
ProductMethyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylateHCID 2759930—

Reaction Steps

Nitroesters 6 and 10 were synthesized from the inexpensive N-methylpyrrole and N-methylimidazole as outlined in Schemes 10 and 11, respectively. Each of these compounds can be prepared economically on a large scale. Methyl 1-methyl-4-nitropyrrole-2-carboxylate (6) was prepared using a modification of the reported synthesis of pyrrole-2-trichloroketone. (Bailey et al. (1971) Org. Syn. 51:101). Briefly, reaction of the inexpensive N-methylpyrrole (14) with trichloroacetylchloride followed by nitration with nitric acid gave nitropyrrole trichloroketone (15), which was treated with sodium methoxide to yield nitropyrrole (6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683189B1
Source datasetuspto-grants-2004_01
ORD IDord-282c938660ab49c392d0855999642d44
Source noteuspto-grants-2004_01