HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845430Generated: October 29, 2026
Potassium Hydroxide → 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid
https://huagongshe.com/reaction/1845430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | methyl 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate | HCID 57826836 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid | HCID 67066099 | — |
Reaction Steps
To a solution of methyl 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate (0.2 g, 0.63 mmol) in THF/H2O (5 mL/1 mL) was added KOH (0.15 g, 2.4 mmol). The reaction mixture was heated to 50° C. for 10 h and then concentrated and diluted with H2O (2 mL). The pH was adjusted to 6 with aqueous HCl. The mixture was extracted with DCM (3×5 mL) and the collected organic fractions were concentrated under vacuum to give crude 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid, which was used directly without further purification. LC-MS (ES) m/z=302 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946278B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b1e0871b26774019826140b5f50931d3 |
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| Source note | uspto-grants-2015_02 |
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