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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8751Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → tert-Butyl 2-(1-oxoprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/8751

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukttert-Butyl 2-(1-hydroxyprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylateHCID 21983945—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl 2-(1-oxoprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylateHCID 2198397384,1%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of oxalyl chloride (1.6 mL, 18.3 mmol) in dichloromethane (150 mL) at −78° C. was slowly added dimethyl sulfoxide (2.6 mL, 37 mmol). After 5 min, a solution of tert-butyl 2-(1-hydroxyprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate (4.75 g, 15.3 mmol) from Step H in dichloromethane (40 mL) was added via an addition funnel. The reaction mixture was stirred for 45 min at −78° C. and then triethylamine (10.2 mL, 73.2 mmol) was added. After 5 min, the reaction mixture was removed from the cooling bath, allowed to warm to room temperature for 1.5 h, poured into water, and extracted three times with dichloromethane. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered and concentrated to afford 4.65 g. The residue was purified by flash chromatography eluting with 15% ethyl acetate in hexanes to give the title compound (3.98 g) as a pink oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091211B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-c0879ba6ad3742769d2b05b03691ff97
Quellennotizuspto-grants-2006_08