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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392205Generated: October 31, 2026

Sodium Hydroxide → 4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-5-methyl-2-furancarboxylic acid

https://huagongshe.com/reaction/2392205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactantmethyl 5-methyl-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylateHCID 57826387—
SolventTetrahydrofuranHCID 8028—
Product4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-5-methyl-2-furancarboxylic acidHCID 57826448100.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

NCS (709 mg, 5.31 mmol) was added in portions to a 150 mL sealed tube reactor containing methyl 5-methyl-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylate (967 mg, 4.39 mmol) in Tetrahydrofuran (THF) (20 mL) at room temperature. The mixture was heated to 70° C. for 1 hour. 6N NaOH (20 mL, 120 mmol) was then added and the mixture stirred at 70° C. for an additional 2 h. The mixture was partitioned between CHCl3 and H2O and the pH of the aqueous phase was adjusted to ˜3 with 6N HCl. The organic layer was separated, dried with Na2SO4 and concentrated affording the title compound (1.13 g, 4.41 mmol, quant.) which was used without further purification: LC-MS (ES) m/z=241 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273782B2
Source datasetuspto-grants-2012_09
ORD IDord-0b1e45bbae124c9ba07d30ffe8922152
Source noteuspto-grants-2012_09