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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 454Erstellt: 24. Oktober 2026

1,4-Dioxa-8-azaspiro(4.5)decane → 8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/de/reaction/454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Edukt3-Bromo-5-methoxypyridineHCID 817163—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelTolueneHCID 1140—
Produkt8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 6674228475,12%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

11/05 2011 07:58:54 +0200 A mixture of 3-bromo-5-methoxypyridine (1.5 g, 7.98 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (1.023 ml, 7.98 mmol), palladium(II) acetate (0.107 g, 0.48 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.228 g, 0.48 mmol) in toluene (38.3 ml) and tBuOH (7.65 ml) was evacuated and flashed with N2 several times. Then sodium 2-methylpropan-2-olate (0.920 g, 9.57 mmol) was added and the reaction mixture was heated to 100°C for 2hrs. LCMS showed complete conversion. Reaction mixture had turned black. The reaction mixture was filtered through celite. The celite was washed with DCM. The combined filtrates were concentrated to yield 2.2g of brown oil, which starts to crystalise patially. Crude NMR showed only little unreacted amine (ca. 14%). The crude was purified by flash: The residue was purified by automated flash chromatography on a 100g column. A gradient from 40% to 100% of EA in Hep over 12CV, 100% EA over 6CV was used as mobile phase. The product was collected using the wavelength 254 nm. 1.5g of desired product were obtained as a light yellow oil.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-7ce32a5d4abb4826b07e10a8720e8cf8
Quellennotiz750 AstraZeneca ELN dataset