HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363319Generated: October 27, 2026
Nitric Acid → 5-Methyl-4-nitrothiophene-2-carboxylic acid
https://huagongshe.com/reaction/1363319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Methylthiophene-2-carboxylic acid | HCID 74713 | — |
| Product | 5-Methyl-4-nitrothiophene-2-carboxylic acid | HCID 3110784 | 70% |
Reaction Steps
Under N2, fuming nitric acid (4.7 mL, 112.0 mmol) was added slowly over 10 min to acetic anhydride (16.6 mL, 175.6 mmol) cooled in a dry ice/acetone bath to −78° C. 5-methyl-2-thiophene carboxylic acid (5.0 g, 35.2 mmol) was added in 1 g portions over 10 min to the solution. The reaction was kept at −20° C. for 1 h before quenching over ice. The yellow solid was filtered off and washed with water (200 mL). The crude product was recrystallized from 95% EtOH to give 5-methyl-4-nitro-2-thiophene carboxylic acid as a pale yellow solid (4.6 g, 70%). 1H NMR (400 MHz, CD3OD) δ (ppm) 8.13 (s, 1H) 2.82 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884124B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-37c9d3f3bbca4700916dad9c3c91c8d5 |
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| Source note | uspto-grants-2011_02 |
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