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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579586Erstellt: 24. Oktober 2026

Water → HCID 178474735, Verbindung

https://huagongshe.com/de/reaction/579586

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
EduktHCID 178446405HCID 178446405—
Katalysator1,2-Bis(diphenylphosphino)ethaneHCID 74267—
KatalysatorHCID 178478077HCID 178478077—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178474735HCID 17847473574,6%

Reaktionsschritte

After stirring for 30 min, a solution of cis-tert-butyl 3-(2-acetamido-1-(tert-butylamino)-1-oxohex-5-en-2-yl)cyclobutyl(benzyl)carbamate (5.34 g, 10.5 mmol), chloro-1,5-cyclooctadiene iridium(I) dimer (212 mg, 0.32 mmol, 3 mol %) and 1,2-bis(diphenylphosphino)ethane (252 mg, 0.63 mmol, 6 mol %) in dichloromethane (50 mL) was cooled to 0° C. and carefully treated with 4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (3.1 mL, 21.1 mmol, 2 eq) over 5 min. After slowly warming to room temperature and stirring overnight, the reaction was poured into water and extracted with ethyl acetate (3×). The combined organic phase was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated. Purification by flash column chromatography (silica gel, 10-40% ethyl acetate in heptane) gave cis-tert-butyl 3-(2-acetamido-1-(tert-butylamino)-1-oxo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexan-2-yl)cyclobutyl(benzyl)carbamate (4.8 g, 7.83 mmol, 74%). ESI MS found for C34H56BN3O6 m/z [614.2 (M+1), 636.2 (M+23)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040703B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-145b60898c134376ae3964236b0ea64a
Quellennotizuspto-grants-2015_05