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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078707Generated: November 1, 2026

Water → 3-iodo-1H-thieno[3,2-c]pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/2078707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178497021HCID 178497021—
SolventTetrahydrofuranHCID 8028—
Product3-iodo-1H-thieno[3,2-c]pyrazole-5-carboxylic acidHCID 17852406850.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-iodo-1H-thieno[3,2-c]pyrazole-5-carboxylic acid methyl ester [4.5 g, 14.60 mmol, Intermediate (26)] in tetrahydrofuran (90 mL) is added potassium hydroxide (2.83 g, 50.44 mmol) and water (20 mL). The resulting reaction mixture is heated at 60° C. oil bath under for 2 hours. The solvent is removed in vacuo and dissolved crude in water (20 mL). The water layer is acidified using 2N hydrochloric acid till pH is 5. White solid precipitated are collected and rinsed with water. The filtrate is extracted three times with ethyl acetate (50 mL). The combined ethyl acetate phases are washed with brine and dried over magnesium sulfate and filtered. Combined solids and stirred in heptane and filtered to obtain 3-iodo-1H-thieno[3,2-c]pyrazole-5-carboxylic acid [2.15 g, 50%, Intermediate (29)] as white solid; 1H NMR [(CD3)2SO)]: δ 13.711 (1H, s), 7.832 (1H, s); LC/MS: 294 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928231B2
Source datasetuspto-grants-2011_04
ORD IDord-f7a3d1190d754ec995fc10898e8e00aa
Source noteuspto-grants-2011_04