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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727442Erstellt: 24. Oktober 2026

Cyclopentene → HCID 18931665, Verbindung

https://huagongshe.com/de/reaction/727442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopenteneHCID 8882—
EduktTriphenylphosphineHCID 11776—
EduktPotassium AcetateHCID 517044—
Edukt2-Amino-5-bromo-3-iodobenzenesulphonic acidHCID 18919385—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 18931665HCID 18931665—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture containing 30 g (79.4 mmol) of 2-amino-5-bromo-3-iodobenzenesulphonic acid, 35 ml (397 mmol) of cyclopentene, 19.5 g (199 mmol) of potassium acetate, 6.24 g (23.8 mmol) of triphenylphosphine and 2.67 g (11.9 mmol) of palladium (II) acetate in 160 ml of N,N-dimethylformamide is heated at 80° C. for 48 hours, under a nitrogen atmosphere. The reaction medium is then concentrated under reduced pressure and the residue is taken up in a mixture containing 200 ml of methanol, 200 ml of 1N hydrochloric acid and 10 ml of 95% sulphuric acid solution. The mixture is evaporated again under reduced pressure and filtered, and the precipitate thus obtained is purified by chromatography on an RP 18 reverse-phase column, eluting with an acetonitrile/water mixture (3:7). The residue is recrystallized from a methanol/pentane mixture.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712393
Quelldatensatzuspto-grants-1998_01
ORD IDord-2b8632528036435e8391493dc5092287
Quellennotizuspto-grants-1998_01