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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402980Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate

https://huagongshe.com/de/reaction/402980

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukttert-butyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamateHCID 2733675—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamateHCID 6998013100,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Oxalyl chloride in anhydrous CH2Cl2 (2.0M, 6.0 mL, 12.0 mmol) was treated with dimethylsulfoxide (1.0 mL, 14.1 mmol) in anhydrous CH2Cl2 (3 mL) dropwise over 5 minutes at −78° C. under a dry N2 atmosphere. The mixture was stirred at −78° C. for 15 minutes and then treated with (2S)-2-(tert-butoxycarbonylamino)-3-phenyl-1-propanol (2.0 g, 8.0 mmol) in anhydrous CH2Cl2 (6 mL) dropwise over 10 minutes. The mixture was stirred at −78° C. for 30 minutes and then treated with triethylamine (4.4 mL, 31.7 mmol) in anhydrous CH2Cl2 (6 mL) dropwise over 10 minutes. The mixture was allowed to slowly warm to ambient temperature, stirred for 1 hour, diluted with CH2Cl2 (100 mL), washed with 10% aqueous citric acid (50 mL), water (50 mL), saturated NaHCO3 (50 mL), dried over Na2SO4, filtered, and the solvent removed under reduced pressure to provide the title compound as an off-white crystalline solid (2.0 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741938B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-22f341aed6f84948bd99d84a2b8abbbe
Quellennotizuspto-grants-2014_06