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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629732Generated: November 3, 2026

Iodine → N-(5-Fluoro-4-iodo-pyridin-3-yl)-2,2-dimethyl-propionamide

https://huagongshe.com/reaction/629732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantN-(5-Fluoropyridin-3-yl)-2,2-dimethylpropanamideHCID 86726332—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-Fluoro-4-iodo-pyridin-3-yl)-2,2-dimethyl-propionamideHCID 86726334100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2.5M solution of nBuLi (30.6 mL, 76 mmol) in hexanes was added drop-wise to a solution of N-(5-fluoropyridin-3-yl)-2,2-dimethylpropanamide 5.0 g, 25.5 mmol) and TMEDA (11.54 mL, 76 mmol) in THF (127 mL) at −78° C. over 1 hour, while ensuring the internal temperature did not go above −70° C. The resulting solution was stirred at −78° C. for 1 hour. Iodine (19.40 g, 76 mmol) in THF (20 mL) was added drop-wise over 30 min ensuring the internal temperature remained below −70° C. The resulting reaction was stirred for 1 hour at −78° C. The reaction was quenched at −78° C. with water and then warmed to ambient temperature. 10% Aqueous sodium thiosulfate was added until the iodine color dissipated and the mixture was extracted with ethyl acetate (×3). The combined organic fractions were dried (MgSO4), filtered and the solvent was evaporated under reduced pressure to afford the title compound (8.21 g, 25.5 mmol, 100% yield), MS (ESI): m/z=323.26 (MH+), 100% pure by LCMS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-9d365d3c13e747609c5791cfa9f0ca6c
Source noteuspto-grants-2016_04