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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2041976Erstellt: 25. Oktober 2026

Benzenesulfonyl chloride → 3-(2-Tert-butylphenoxy)-1-(phenylsulfonyl)azetidine

https://huagongshe.com/reaction/2041976

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
Edukt3-(2-Tert-butylphenoxy)azetidineHCID 53409530—
LösungsmittelPyridineHCID 1049—
Produkt3-(2-Tert-butylphenoxy)-1-(phenylsulfonyl)azetidineHCID 5957731757,5%

Reaktionsschritte

To a stirred solution of 3-(2-tert-butylphenoxy)azetidine (0.30 g, 1.46 mmol) in pyridine (5.0 mL) was added benzenesulfonyl chloride (0.28 g, 1.61 mmol). After stirring for 16 h at room temperature, the reaction mixture was concentrated under reduced pressure and the residue was dissolved in ethyl acetate. The organic layer was washed with 1.0 N hydrochloric acid, water, saturated sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The resulting yellow solid was recrystallized from heptane/ethyl acetate to provide 3-(2-tert-butylphenoxy)-1-(phenylsulfonyl)azetidine (0.29 g, 57%) as a pale brown powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08586571B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-5ef943e2899746cdaeedcbc1c7011ce7
Quellennotizuspto-grants-2013_11