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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660197Erstellt: 25. Oktober 2026

Diethyl Ether → (S)-Methyl 4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate

https://huagongshe.com/reaction/660197

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
Edukt(S)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamateHCID 56973617—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
Produkt(S)-Methyl 4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoateHCID 5743229794%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of tert-butyl[(1S)-1-(4-bromophenyl)ethyl]carbamate (step 3, 14.73 g, 49.1 mmol), 1,3-bis(diphenylphosphino)-propane (2.03 g, 4.91 mmol), palladium (II) acetate (1.10 g, 4.91 mmol), triethylamine (20.5 mL, 147 mmol), N,N-dimethylforamide (120 mL) and methanol (180 mL) was stirred at 80° C. for 16 h under carbon monoxide atmosphere. After cooling to room temperature, the mixture was diluted with ether (800 mL) and washed with water (500 mL×3). The organic layer was dried over magnesium sulfate and evaporated. The residue was purified by flush column chromatography on silica gel eluting with hexane/ethyl acetate (5:1) to afford 12.83 g (94%) of the title compound as white solids:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084476B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-74ed380daa874011a8c51b77913037c9
Quellennotizuspto-grants-2011_12