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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951295Generated: November 2, 2026

Hydrochloric Acid → methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochloride

https://huagongshe.com/reaction/1951295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantO-(2,4-dinitrophenyl)hydroxylamineHCID 87140—
ReactantMethyl 3-chloro-1H-pyrrole-2-carboxylateHCID 5324605—
SolventDiethyl EtherHCID 3283—
SolventSodium ChlorideHCID 5234—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Productmethyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochlorideHCID 67017160—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of methyl 3-chloro-1H-pyrrole-2-carboxylate (2.50 g, 15.7 mmol) and DMF (10 mL) at 0° C. was added 60% sodium hydride (0.816 g, 20.4 mmol). After 15 min, O-(2,4-dinitrophenyl)hydroxylamine (3.74 g, 18.8 mmol) was added and the mixture was stirred at 0° C. for 1 hr before warming to RT. After 18 hrs, the mixture was diluted with 10% NaCl and extracted with EtOAc. The organic fractions were dried with sodium sulfate and purified by silica gel chromatography using 10-30% Hexanes:EtOAc to afford a crude, brown oil. The oil was taken up in Et2O and treated with 4 N HCl in dioxane. The resulting off-white precipitate was collected by filtration to afford methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404694B2
Source datasetuspto-grants-2013_03
ORD IDord-17bd3ab921994157b47ec7bc2710d396
Source noteuspto-grants-2013_03