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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436069Generated: October 30, 2026

Stannane, tributyl(1-ethoxyethenyl)- → 4-Acetyl-2-fluorobenzonitrile

https://huagongshe.com/reaction/1436069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
Product4-Acetyl-2-fluorobenzonitrileHCID 2248165311.6%

Reaction Steps

A mixture of 4-bromo-2-fluorobenzonitrile (10.6 g, 52.8 mmol), tributyl(1-ethoxyvinyl)tin (21 g, 58.1 mmol), and trans-dichlorobis(triphenylphosphine)palladium (II) (371 mg, 0.53 mmol) in 190 mL of dry toluene were refluxed for 2 h and then quenched with 5% HCl and stirred for 30 min. Ethyl acetate was added and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 6.5 g of crude product. Purification of the product on silica gel using 5% ethyl acetate:hexane gave 4-acetyl-2-fluorobenzonitrile (1.0 g, 11%), MS (ES) m/z 164 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618989B2
Source datasetuspto-grants-2009_11
ORD IDord-769443de1c7049999a04e438c0a0a619
Source noteuspto-grants-2009_11