Reaktion #2954

ord-9cef4a5077a74084b0f66091336f0c5e

Reaktionsgleichung

COc1cccc([C@]23CCNC[C@@H]2CCC(=O)C3)c1.Cl
(±)-trans-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride
CCCCBr
butyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[K+]
potassium iodide
CCCCN1CC[C@]2(c3cccc(OC)c3)CC(=O)CC[C@H]2C1
title compound
Ausbeute 24.9%
CCCCN1CC[C@]2(c3cccc(OC)c3)CC(=O)CC[C@H]2C1
(±)-trans-2-Butyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline
Ausbeute 24.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeas described in preparation 20

Vorschrift

0.71 g (2.55 mmol) of (±)-trans-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride, 0.37 g (2.68 mmol) of butyl bromide, 0.53 g of potassium carbonate and a catalytical amount of potassium iodide in 15 ml of DMF were reacted as described in preparation 20, yielding 0.2 g of the title compound which was used as such in the subsequent step.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731322uspto-grants-1998_03