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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472771Generated: October 25, 2026

Potassium Fluoride → 4-Bromo-5-(4-methylnaphthalen-1-yl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/1472771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant4-Methyl-1-naphthaleneboronic acidHCID 2773511—
Reactant4,5-Dibromothiophene-2-carbonitrileHCID 23262276—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product4-Bromo-5-(4-methylnaphthalen-1-yl)thiophene-2-carbonitrileHCID 6829362288.4%

Reaction Steps

A round-bottomed flask was charged with 4,5-dibromothiophene-2-carbonitrile (536 mg, 2.00 mmol), 4-methylnaphthalen-1-ylboronic acid (409 mg, 2.20 mmol), Pd2(dba)3 (18.3 mg, 0.020 mmol) and KF (383 mg, 6.60). After degassed, dioxane (5 mL) and P(Bu-t)3 (0.24 mL, 0.2M, 0.048 mmol) was added. The reaction mixture was stirred at rt until complete. 30 mL of water was added, and the reaction mixture was extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulphate and then concentrated. The residue was purified by flash chromatography (hexane:CH2Cl2=3:1). 0.58 g (88%) of product was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012655B2
Source datasetuspto-grants-2015_04
ORD IDord-99eaff835a184249a65a657b5e3a0282
Source noteuspto-grants-2015_04