Reaktion #1093371

ord-f0348b31ac4940c3a96ce13ccb7ff005

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigegave, after 3 d at 0° C.
  2. 2
    workup.DISTILLATIONKugelrohr distillation (0.4 torr, 220° C.)

Vorschrift

General procedure B using (S)-p-tol-BINAP and 3-isopropylcyclopentenone (0.11 g, 0.9 mmol) gave, after 3 d at 0° C. and Kugelrohr distillation (0.4 torr, 220° C.) followed by flash chromatography (10:1 pentane:diethyl ether), the title compound as a clear liquid (0.10 g, 89% yield). In addition to the desired product, starting material (0.011 g, 10%) was also isolated. Spectroscopic data for the title compound were consistent with previously reported data.16 [α]D25° C.−200° (c 1.6, CHCl3) (lit.16 [α]D25° C.−110° (c 1.0, CHCl3) for 60% ee). Chiral GC analysis (Chiraldex G-TA column) indicated that the title compound was obtained in 95% ee.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06787655B2uspto-grants-2004_09