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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237295Erstellt: 25. Oktober 2026

Triethylamine → 3-[5-Bromo-2-(3-fluoro-benzyloxy)-phenoxy]-1-tert-butyl-azetidine

https://huagongshe.com/reaction/237295

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPotassium CarbonateHCID 11430—
Edukt1-tert-Butyl-3-hydroxyazetidineHCID 287986—
EduktMeSO3ClHCID 12750509—
Edukt5-Bromo-2-(3-fluoro-benzyloxy)-phenolHCID 67348159—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-[5-Bromo-2-(3-fluoro-benzyloxy)-phenoxy]-1-tert-butyl-azetidineHCID 5840506192,6%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of the title compound of Step A (3 mmol), and triethylamine (6 mmol) in CH2Cl2 (50 mL), was added MeSO3Cl (4 mmol). The mixture was stirred at 25° C. for 16 h. After concentration, ⅓ of the residue was dissolved in MeCN (20 mL). Next, 5-bromo-2-(3-fluoro-benzyloxy)-phenol (0.5 mmol) and K2CO3 (2 mmol) were added. The mixture was stirred at 100° C. for 16 h, concentrated and purified via PTLC providing the title compound (189 mg). MS (ESI): mass calcd. for C20H23BrFNO2, 407.1; m/z found, 408.0 [M+H]+. 1H NMR (CDCl3): 7.37-7.28 (m, 1H), 7.19-7.12 (m, 2H), 7.04-6.95 (m, 2H), 6.84-6.63 (m, 2H), 5.08 (s, 2H), 4.78-4.48 (m, 1H), 3.68-3.62 (m, 2H), 3.35-3.26 (m, 2H), 1.00 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642583B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-aa6463d549f84e12a53050ba26241be7
Quellennotizuspto-grants-2014_02