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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | O-(2,4-dinitrophenyl)hydroxylamine | HCID 87140 | — |
| Reactant | Methyl 3-chloro-1H-pyrrole-2-carboxylate | HCID 5324605 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochloride | HCID 67017160 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404694B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-17bd3ab921994157b47ec7bc2710d396 |
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| Source note | uspto-grants-2013_03 |
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