Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1025321Erstellt: 24. Oktober 2026

Benzoxazole → tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamate

https://huagongshe.com/de/reaction/1025321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoxazoleHCID 9228—
EduktAmmonium ChlorideHCID 25517—
Edukttert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamateHCID 11522383—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

Under an atmosphere of argon, benzo[d]oxazole (5 g, 42.0 mmol, Eq: 1.00) was combined with THF (100 ml) to give a light yellow solution. At −5° C. isopropylmagnesium chloride 2M in THF (21.0 ml, 42.0 mmol, Eq: 1.00) was added dropwise. The reaction was stirred for 1.5 h at −5° C. Then (S)-tert-butyl 1-oxobutan-2-ylcarbamate (4.72 g, 25.2 mmol, Eq: 0.6) diluted in 20 ml THF was added. The reaction was stirred overnight at RT. Satd. ammoniumchloride solution (6 ml) was added to the reaction. The THF was evaporated under vacuum. The reaction mixture was poured into 50 ml H2O and extracted with ethyl acetate (2×100 ml). The crude material was purified by flash chromatography (silica gel, 20 g, 0% to 40% ethyl acetate in heptane). The title compound was obtained as a brown gum (5.08 g, 39.5%, MS (m/e)=307.2 [M+H+]).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08729061B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-545695dd0df944b9b559205a855afc46
Quellennotizuspto-grants-2014_05