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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21001Erstellt: 25. Oktober 2026

Ammonium fluoride → 3-Amino-4-(thiophen-2-yl)-6-bromophthalimide

https://huagongshe.com/reaction/21001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium fluorideHCID 25516—
Edukt2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Edukt3-Amino-4-iodo-6-bromophthalimideHCID 68488717—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Amino-4-(thiophen-2-yl)-6-bromophthalimideHCID 6848938287,3%

Reaktionsschritte

3-Amino-4-iodo-6-bromophthalimide (100 mg, 0.273 mmol) was dissolved in THF (5 mL), and the solution was added with 2-(tributylstannyl)thiophene (0.173 mL, 0.546 mmol) and bis(triphenylphosphine)dichloropalladium (15 mg, 0.022 mmol), followed by stirring under reflux for 12.5 hours under argon atmosphere. The reaction mixture was added with 10% aqueous ammonium fluoride solution, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by slurry using hexane, then purified by preparative thin-layer chromatography (chloroform/acetonitrile=30/1) to obtain 3-amino-4-(thiophen-2-yl)-6-bromophthalimide (77 mg, yield 87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-bd1d487b26d04c6bb41832b318163851
Quellennotizuspto-grants-2010_06