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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727436Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Amino-5-bromo[1,1'-biphenyl]-3-sulphonic acid

https://huagongshe.com/de/reaction/727436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfuric AcidHCID 1118—
EduktSodium CarbonateHCID 10340—
EduktPhenylboronic AcidHCID 66827—
Edukt2-Amino-5-bromo-3-iodobenzenesulphonic acidHCID 18919385—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2-Amino-5-bromo[1,1'-biphenyl]-3-sulphonic acidHCID 18931667—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of 37.8 g (100 mmol) of 2-amino-5-bromo-3-iodobenzenesulphonic acid and 32 g (300 mmol) of sodium carbonate in 300 ml of 1,2-dimethoxyethane and 150 ml of water are successively added, under a nitrogen atmosphere, 5.8 g (5 mmol) of tetrakis(triphenylphosphine)palladium (0) and 19.5 g (160 mmol) of benzeneboronic acid. The mixture is heated at the reflux temperature for 4 hours and the reaction medium is then concentrated under reduced pressure. The residue thus obtained is then dissolved in a mixture containing 300 ml of methanol, 300 ml of 0.1N hydrochloric acid and 16 ml of 95% sulphuric acid. The mixture is concentrated to 100 ml under reduced pressure, cooled to 0° C. and filtered. The residue is purified by chromatography on an RP 18 reverse-phase column, eluting with an acetonitrile:water mixture (2:8).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712393
Quelldatensatzuspto-grants-1998_01
ORD IDord-9d0f647a178945ec88aa837ce90d1f64
Quellennotizuspto-grants-1998_01