5-(Benzyloxy)-2-diazonio-1-methoxy-3-oxohepta-1,6-dien-1-olate → HCID 53869755, Verbindung

HRID 839277Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 839277
[CH3:1][O:2][C:3](=[O:21])[C:4](=[N+]=[N-])[C:5](=[O:18])[CH2:6][CH:7]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:8]=[CH2:9]>C1(C)C(C)=CC=CC=1>[CH3:1][O:2][C:3]([C:4]12[CH2:9][CH:8]1[CH:7]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:6][C:5]2=[O:18])=[O:21]

Komponenten

3

Versuchsvorschrift

In accordance with the process of Preparation 22, 5-benzyloxy-2-diazo-3-oxo-6-heptenoic acid methyl ester (1.16 g; 4 mmol) and copper acetylacetone complex (100 mg) were dissolved in 30 ml of anhydrous xylene. The reaction product was purified by silica gel column chromatography to obtain two types of isomers of 4-benzyloxy-2-oxo-bicyclo[3.1.0] hexane-1-carboxylic acid methyl ester (248mg) as an oily product.

Aufarbeitung

  1. customThe reaction product was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-ba22bac3efe54a6bb169f74dee7473b0
Quelldatensatz
uspto-grants-1978_06
Patentnummer
US04094886

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