HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238714Generated: October 26, 2026
Hydrochloric Acid → 4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid
https://huagongshe.com/reaction/238714
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-2-thiophenecarboxylic Acid | HCID 610409 | — |
| Reactant | 2-(2-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 57483800 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid | HCID 57483844 | 133.4% |
Reaction Steps
2-(2-Methoxy-3-nitro-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 4d (0.81 g, 2.9 mmol), 4-bromo-thiophene-2-carboxylic acid (0.3 g, 1.45 mmol), tetrakis (triphenylphosphine)palladium (80 mg, 0.073 mmol) and sodium carbonate (0.31 g, 2.9 mmol) were dissolved in a solvent mixture of 20 mL of 1,4-dioxane and 10 mL of water. The reaction was heated to reflux for 0.5 hours. The mixture was adjusted to pH 3 with 1 N hydrochloric acid and extracted with ethyl acetate (20 mL×3). The combined organic extracts were concentrated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound 4-(3-nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid 19a (0.54 g) as a brown oil, which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642637B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-6b75d065aaba43979d898ef8c12a5b3e |
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| Source note | uspto-grants-2014_02 |
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