Synthesis of 5‐Methoxy‐ and 5‐(Dialkylamino)bicyclo[3.2.0]hept‐2‐en‐6‐one Derivatives by cine Substitution with Methoxide Anions and Dialkylamines

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OriginalspracheEnglisch
Seiten (von - bis)137-144
Seitenumfang8
FachzeitschriftChemische Berichte
Jahrgang127
Ausgabenummer1
PublikationsstatusVeröffentlicht - Jan. 1994
Extern publiziertJa

Abstract

exo‐7‐Chloro‐endo‐7‐phenylbicyclo[3.2.0]hept‐2‐en‐6‐one (5) undergoes cine substitution reactions with methoxide anions and with dialkylamines to give 5‐methoxy or 5‐dialkylamino derivatives 13, 14, 16–19 in high yield. While attempts directed to an acetalization have failed, the addition of Grignard reagents to the methoxy derivatives proceeds stereoselectively in high yield. Hydrochlorides 20/21 lose amine at 110°C to form 2‐phenyltropone 22. Thermolysis of diethylamino derivative 24 at 170°C (temperature determined by DSC) results in the formation of the dienaminone 25.

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Synthesis of 5‐Methoxy‐ and 5‐(Dialkylamino)bicyclo[3.2.0]hept‐2‐en‐6‐one Derivatives by cine Substitution with Methoxide Anions and Dialkylamines. / Butenschön, Holger.
in: Chemische Berichte, Jahrgang 127, Nr. 1, 01.1994, S. 137-144.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Synthesis of 5‐Methoxy‐ and 5‐(Dialkylamino)bicyclo[3.2.0]hept‐2‐en‐6‐one Derivatives by cine Substitution with Methoxide Anions and Dialkylamines",
abstract = "exo‐7‐Chloro‐endo‐7‐phenylbicyclo[3.2.0]hept‐2‐en‐6‐one (5) undergoes cine substitution reactions with methoxide anions and with dialkylamines to give 5‐methoxy or 5‐dialkylamino derivatives 13, 14, 16–19 in high yield. While attempts directed to an acetalization have failed, the addition of Grignard reagents to the methoxy derivatives proceeds stereoselectively in high yield. Hydrochlorides 20/21 lose amine at 110°C to form 2‐phenyltropone 22. Thermolysis of diethylamino derivative 24 at 170°C (temperature determined by DSC) results in the formation of the dienaminone 25.",
keywords = "Bicyclo[3.2.0]hept‐2‐en‐6‐one, cine substitution, DSC",
author = "Holger Butensch{\"o}n",
year = "1994",
month = jan,
doi = "10.1002/cber.19941270122",
language = "English",
volume = "127",
pages = "137--144",
journal = "Chemische Berichte",
issn = "0009-2940",
publisher = "Wiley-VCH Verlag",
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Download

TY - JOUR

T1 - Synthesis of 5‐Methoxy‐ and 5‐(Dialkylamino)bicyclo[3.2.0]hept‐2‐en‐6‐one Derivatives by cine Substitution with Methoxide Anions and Dialkylamines

AU - Butenschön, Holger

PY - 1994/1

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AB - exo‐7‐Chloro‐endo‐7‐phenylbicyclo[3.2.0]hept‐2‐en‐6‐one (5) undergoes cine substitution reactions with methoxide anions and with dialkylamines to give 5‐methoxy or 5‐dialkylamino derivatives 13, 14, 16–19 in high yield. While attempts directed to an acetalization have failed, the addition of Grignard reagents to the methoxy derivatives proceeds stereoselectively in high yield. Hydrochlorides 20/21 lose amine at 110°C to form 2‐phenyltropone 22. Thermolysis of diethylamino derivative 24 at 170°C (temperature determined by DSC) results in the formation of the dienaminone 25.

KW - Bicyclo[3.2.0]hept‐2‐en‐6‐one, cine substitution

KW - DSC

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DO - 10.1002/cber.19941270122

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JO - Chemische Berichte

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