HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18932Generated: October 25, 2026
Hydrochloric Acid → 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acid
https://huagongshe.com/reaction/18932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | methyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylate | HCID 18322358 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acid | HCID 18322391 | 64.3% |
Reaction Steps
A solution of LiOH monohydrate (0.083 g, 2.0 mmol) in water (1 mL) was added to a solution of methyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylate (0.150 mL, 0.66 mmol) in THF:MeOH (3:1, 3 mL) and the resulting mixture heated at 75° C. for 5 hours. The reaction was cooled down to room temperature and acidified with 1N aqueous HCl, extracted with ethyl acetate. The combined organic layers were dried, the solvent eliminated under vacuum and the crude product recrystallized from dichloromethane:hexane to afford 90 mg of expected 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acid as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741479B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-7453776a39e54e01a5ebd772ea3e57f2 |
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| Source note | uspto-grants-2010_06 |
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