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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511275Generated: November 2, 2026

Ethanol → 3-(4-Iodo-1H-pyrazol-1-yl)cyclobutanol

https://huagongshe.com/reaction/511275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-iodo-1H-pyrazol-1-yl)cyclobutan-1-oneHCID 67254778—
Product3-(4-Iodo-1H-pyrazol-1-yl)cyclobutanolHCID 6725402594.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(4-Iodo-pyrazol-1-yl)cyclobutanone (Compound 100D, 1.000 g, 3.816 mmol), sodium borohydride (145.8 mg, 3.854 mmol) and ethanol (22.28 mL, 381.6 mmol) were added to a round bottom flask and the reaction mixture was stirred at 0° C. for 3 h. Reaction mixture was concentrated in vacuo and washed with water extracting with DCM. The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo to afford 956 mg of the final compound as colorless oil. Compound was taken on to the next step without further purification. MS (ES+): m/z 264.86 (100) [MH+]; HPLC: tR=2.50 min (Polar—5 min, ZQ3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096624B2
Source datasetuspto-grants-2015_08
ORD IDord-669eb04e50fd463a84a95853cab1bf27
Source noteuspto-grants-2015_08