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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173218Generated: October 31, 2026

Allyltributylstannane → 2-Chloro-6-fluoro-3-(prop-2-en-1-yl)benzonitrile

https://huagongshe.com/reaction/2173218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
ReactantLithium ChlorideHCID 433294—
Reactant2-Chloro-6-fluoro-3-iodobenzonitrileHCID 67515812—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-6-fluoro-3-(prop-2-en-1-yl)benzonitrileHCID 67516122—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-6-fluoro-3-iodobenzonitrile (800 mg, 2.85 mmol), allyltributylstannane (1.245 mg, 3.761 mmol), LiCl (431 mg, 10.3 mmol) and Pd(PPh3)4 (100 mg) in 50 mL toluene was heated at 100° C. overnight. Cooled to rt. and diluted with 50 mL EtOAc and filtered. The filtrate was washed with water and brine, dried over anhydrous Na2SO4 and concentrated to dryness. The residue was purified via prep-TLC (ethyl acetate/Pet ether=1:5) to give 2-chloro-6-fluoro-3-(prop-2-en-1-yl)benzonitrile. 1H-NMR (400 MHz, CDCl3) δ ppm 7.37˜7.41 (m, 1H), 7.01˜7.06 (m, 1H), 5.78˜5.87 (m, 1H), 4.99˜5.12 (m, 2H), 3.44 (d, J=6.3 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-89c893a53f09414da9ab3ace5c8ace6c
Source noteuspto-grants-2015_06