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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 356772Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/356772

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 699801385,1%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To dimethyl sulfoxide (2.82 mL, 39.8 mmol) dissolved in anhydrous methylene chloride (5 mL) and cooled to -78° C. was added dropwise oxalyl chloride (2.6 mL, 1.5 equiv). After 10 minutes at -78° C., N-Boc-Phenylalaninol (5.00 g, 19.9 mmol) dissolved in anhydrous methylene chloride (75 mL) was cannulated into the reaction mixture. After 15 minutes at -78° C., the reaction was stirred for 2 minutes at 0° C. and then cooled again to -78° C. Triethylamine (11.9 mL, 4.3 equiv) was added dropwise. After 25 minutes, the reaction was quenched with cooled 10% citric acid (15 mL) and then diluted with additional 10% citric acid (75 mL). Ether (300 mL) was added and the solution was washed with water (5×100 mL), brine, water (5×100 mL), and brine, dried over sodium sulfate, and concentrated under reduced pressure to afford the title compound (4.22 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05837873
Quelldatensatzuspto-grants-1998_11
ORD IDord-7c739f3178ab4503a190a6bb0d53e316
Quellennotizuspto-grants-1998_11