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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880553Generated: November 2, 2026

Iodine → (3R)-3-(4-Bromo-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile

https://huagongshe.com/reaction/880553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium HydroxideHCID 14923—
Reactant(R)-3-(4-bromo-1H-pyrazol-1-yl)-3-cyclopentylpropanalHCID 59420157—
SolventWaterHCID 962—
Product(3R)-3-(4-Bromo-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrileHCID 6847408979.3%

Reaction Steps

To a stirred solution of (3R)-3-(4-bromo-1H-pyrazol-1-yl)-3-cyclopentylpropanal ((R)-40, 230.5 mg, 0.85 mmol) in tetrahydrofuran (THF, 2.4 mL, 29 mmol) at room temperature was added a solution of 14.3 M of ammonium hydroxide (NH4OH) in water (2.4 mL), followed by iodine (I2, 237 mg, 0.935 mmol, 1.1 equiv). The resulting reaction mixture was stirred at room temperature for 30 min. When LCMS showed that the reaction was complete, the reaction mixture was quenched with 10% aqueous Na2S2O3 solution (15 mL) and extracted with EtOAc (2×15 mL). The combined organic layers were washed with brine, dried over magnesium sulfate (MgSO4), filtered, and concentrated under reduced pressure. The residue was purified by Combiflash (SiO2) with 0-30% EtOAc/hexane gradient elution to give (3R)-3-(4-bromo-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile ((R)-41, 180.7 mg, 227.9 mg theoretical, 79.3% yield) as a colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993582B2
Source datasetuspto-grants-2015_03
ORD IDord-a6f4050fc8594fb3b270e5d0d4ceb082
Source noteuspto-grants-2015_03