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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 428320Erstellt: 24. Oktober 2026

Vinyl isobutyl ether → HCID 54165959, Verbindung

https://huagongshe.com/de/reaction/428320

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVinyl isobutyl etherHCID 7992—
EduktTriethylamineHCID 8471—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
Edukt(R)-3-(2-benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amineHCID 24885301—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 54165959HCID 54165959—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a stirred solution of (R)-N,N-diisopropyl-3-(2-benzyloxy-5-bromophenyl)-3-phenylpropanamine (Example 12) (10.2 g, 21.23 mmol) in DMF (100 mL) under nitrogen atmosphere at room temperature were sequentially added triethylamine (2.58 g, 25.47 mmol), TlOAc (6.15 g, 23.35 mmol), isobutylvinylether (14 mL, 106.14 mmol), DPPP (0.87 g, 2.12 mmol) and Pd(OAc)2 (0.24 g, 1.06 mmol). The reaction temperature was raised to 100° C. and stirred for 3 hours, cooled to room temperature, filtered and treated with HCl (5%, 250 mL) and stirred for another 2 hours. The reaction mixture was repeatedly extracted with dichloromethane and the combined organic layers were dried (MgSO4), filtered and the solvent evaporated. Triethylamine and DMF were destined off under reduced pressure to yield 9 g (98%); 1H NMR (CDCl3) δ1.22 (m, 12H), 2.52-2.70 (m, 7H), 3.40 (br, 2H), 4.34 (t, 1H), 5.10 (s, 1H), 6.90 (d, 1H), 7.17-7.40 (m, 10H), 7.82 (m, 1H) and 7.92 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313132B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-1c4499c960ae4932a4e9ac8d078bc00c
Quellennotizuspto-grants-2001_11