Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096970Generated: October 31, 2026

Iodine → 2-Fluoro-3-iodobenzonitrile

https://huagongshe.com/reaction/2096970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantSodium ThiosulfateHCID 24477—
Reactant2-FluorobenzonitrileHCID 67855—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-3-iodobenzonitrileHCID 5815427687%

Reaction Conditions

Temperature-50 °C

Reaction Steps

n-Butyl lithium (2.5 M in hexanes, 16.8 mL, 42 mmol) was added dropwise to a stirred solution of 2,2,6,6-tetramethylpiperidine (6.90 mL, 141 mmol) in tetrahydrofuran (60 mL) at −78° C. The mixture was stirred for 30 minutes at −50° C. then 2-fluorobenzonitrile (4.4 g, 37 mmol) in tetrahydrofuran (25 mL) was added dropwise to the mixture at −78° C. The reaction was warmed to −50° C. over a 30 minute period and then recooled to −78° C. and a solution of iodine (10.20 g, 40 mmol) in tetrahydrofuran (25 mL) was added. Then the mixture was warmed to ambient temperature. After 1 hour, saturated aqueous sodium thiosulphate solution was added to the reaction and the mixture was extracted with diethyl ether. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. Purification of the residue by flash chromatography (20:1 hexanes/ethyl acetate) gave the title compound (7.86 g, 87%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450341B2
Source datasetuspto-grants-2013_05
ORD IDord-802ddbf0d674417888f189b905af6f4c
Source noteuspto-grants-2013_05