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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579505Erstellt: 23. Oktober 2026

HCID 66832833, Verbindung → HCID 66833605, Verbindung

https://huagongshe.com/de/reaction/579505

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHCID 66832833HCID 66832833—
EduktHCID 178419189HCID 178419189—
Katalysator1,2-Bis(diphenylphosphino)ethaneHCID 74267—
KatalysatorChloro(1,5-cyclooctadiene)iridium(I) dimerHCID 6436381—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 66833605HCID 6683360565,3%

Reaktionsschritte

While under an argon atmosphere, a solution of chloro(1,5-cyclooctadiene) iridium(I) dimer (15 mg, 0.022 mmol) and 1,2-bis(diphenyl-phosphino) ethane (18 mg, 0.044 mmol) in dichloromethane (5 mL) was treated with pinacol borane (225 mg, 1.76 mmol, 0.26 mL) and stirred for 15 minutes. To this mixture was added a solution of 3-benzyl 4-ethyl 4-(but-3-enyl)-2,2-dimethyloxazolidine-3,4-dicarboxylate (530 mg, 1.47 mmol) in dichloromethane (5 mL). After stirring for 19 h at room temperature the solution was concentrated and purified using a combiflash system (24 g column, eluting with 5-50% (ethyl acetate in heptanes) to give 3-benzyl 4-ethyl 2,2-dimethyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl)oxazolidine-3,4-dicarboxylate (470 mg, 65%). 1H NMR (CDCl3) δ: 7.22 (m, 5H), 5.01 (m, 2H), 3.91 (m, 4H), 2.20-2.01 (m, 1H), 1.75 (m, 1H), 1.51 (2s, 6H), 1.29 (m, 4H), 1.16 (s, 12H), 1.02 (t, J=7.2 Hz, 3H), 0.69 (t, 2H). MS found for C26H40BNO7 m/z [490 (M+1), 522 (M+Na)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040703B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-e47af45f283f4e74866134f98b723080
Quellennotizuspto-grants-2015_05