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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactantmethyl 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylateHCID 57826836—
SolventOxolane--water (1/1)HCID 21881883—
Product4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acidHCID 67066099—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946278B2
Source datasetuspto-grants-2015_02
ORD IDord-b1e0871b26774019826140b5f50931d3
Source noteuspto-grants-2015_02