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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42142Erstellt: 23. Oktober 2026

Ammonium Chloride → 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine

https://huagongshe.com/de/reaction/42142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2,5-DibromopyridineHCID 69353—
Edukt(4-Methanesulfonylphenyl)methanolHCID 3801026—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridineHCID 6708325631%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 2,5-dibromopyridine (474 mg, 2.00 mmol) and 4-(methanesulfonyl)benzyl alcohol (372 mg, 2.00 mmol) in tetrahydrofuran (5 mL) was cooled to −15° C. under N2 and potassium tert-butoxide (1.0M in tetrahydrofuran, 2.2 mL, 2.20 mmol) was added dropwise over 10 minutes. The mixture was stirred at 0° C. for 5.5 hours, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give the title compound (210 mg, yield 31%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536176B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c78bc94182cb42c48b59f4800f97a3c8
Quellennotizuspto-grants-2013_09