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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1253327Erstellt: 27. Oktober 2026

Acetonitrile → 8-(4-(Methylsulfonyl)phenyl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/1253327

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktPotassium CarbonateHCID 11430—
Edukt1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Edukt1-Fluoro-4-(methylsulphonyl)benzeneHCID 67994—
LösungsmittelWaterHCID 962—
Produkt8-(4-(Methylsulfonyl)phenyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 425636077,3%

Reaktionsschritte

A mixture of 10 g (0.057 mol) of p-fluorophenyl methyl sulfone, 8.72 g (0.063 mol) of K2CO3, 24.66 g (0.172 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, and 50 ml of acetonitrile is stirred overnight at 90°-100° C. After cooling, the mixture is diluted with water and extracted with methylene chloride. The combined extracts are washed with brine, dried over Na2SO4, and concentrated in vacuo. Trituration with ether affords 13.11 g (77%) of title compound as a white solid: m.p. 192°-194° C.; IR (KBr) 1588, 1369, and 1290 cm-1 ; NMR (CDCl3) δ 7.74 (m, 2H), 6.96 (m, 2H), 4.02 (s, 4H), 3.54 (m, 4H), 3.03 (s, 3H), 1.81 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04748246
Quelldatensatzuspto-grants-1988_05
ORD IDord-b36c1ff0aa1544ee989519f9babb580b
Quellennotizuspto-grants-1988_05