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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078735Generated: October 27, 2026

Iodine → HCID 178519291, compound

https://huagongshe.com/reaction/2078735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BisulfiteHCID 23665763—
Reactant(1H-Thieno[3,2-c]pyrazol-5-yl)methanolHCID 57354336—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178519291HCID 17851929191%

Reaction Steps

To a solution of (1H-thieno[3,2-c]pyrazol-5-yl)-methanol [3.2 g, 20.8 mmol, Intermediate (70)] in solution in dimethyl formamide (40 mL) were added potassium hydroxide (3.5 g, 62.3 mmol) and iodine (7.9 g, 31.1 mmol). The mixture was stirred at room temperature for 5 hours. A concentrated solution of sodium bisulfite in water was added until the orange color disappeared. The resulting mixture was extracted several times with ethyl acetate. The combined organic layers were dried over magnesium sulfate and concentrated. The residue was triturated in dichloromethane to produce (3-iodo-1H-thieno[3,2-c]pyrazol-5-yl)-methanol [5.3 g, 91%, Intermediate (71)]. LC/MS: 280.91 (M+H), RT=1.93 minutes; 1H NMR [300 Mhz, (CD3)2SO]: δ13.23 (s, 1H), 7.12 (s, 1H), 5.64 (t, J=6.6 Hz, 1H), 4.63 (d, J=6.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928231B2
Source datasetuspto-grants-2011_04
ORD IDord-e05bbc791edc4245abb6d8f3653dc6c3
Source noteuspto-grants-2011_04