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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29189Erstellt: 23. Oktober 2026

Isopropanol → tert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamate

https://huagongshe.com/de/reaction/29189

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktDiisopropylethylamineHCID 81531—
EduktO-tert-butylhydroxylamine hydrochlorideHCID 2777906—
Edukt(1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamateHCID 20638362—
Produkttert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamateHCID 59090702—

Reaktionsschritte

tert-Butyl-N-((1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamate (0.155 g, 0.59 mmol) and O-(tert-butyl)hydroxylamine hydrochloride (0.089 g, 0.71 mmol) were heated with diisopropylethylamine (0.154 ml, 0.88 mmol) in isopropanol (2 ml) in a sealed tube at 60° C. for 5 days. The reaction mixture was concentrated in vacuo, taken up in EtOAc, washed with sat. aq. NaHCO3, and brine. The organic phase was dried over MgSO4, filtered and solvent removed in vacuo. Purication by column chromatography (1% MeOH in CH2Cl2) gave 100 mg of a white solid which was used directly in the next reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419967B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-52b8f8f029684768afcaa2b5b52f915e
Quellennotizuspto-grants-2008_09