HCID 86702657, Verbindung → HCID 86702656, Verbindung
Reaktionsgleichung
[C:1]1(/[CH:7]=[CH:8]/[CH2:9][CH2:10][CH2:11][C:12]#[C:13][C:14](=[O:20])[CH2:15][CH2:16][CH:17]=[C:18]=[CH2:19])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>ClC1C=CC=CC=1Cl>[CH2:9]1[C:8]2=[CH:7][C:1]3[C:6]([C:13]([C:14](=[O:20])[CH2:15][CH2:16][CH:17]=[C:18]=[CH2:19])=[C:12]2[CH2:11][CH2:10]1)=[CH:5][CH:4]=[CH:3][CH:2]=3Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 225 °C
Versuchsvorschrift
To a 2-5 mL MWI vial equipped with a stir bar was added the ene-allene-yne 1 (50 mg, 0.19 mmol) in o-dichlorobenzene (2.5 mL), and the reaction was irradiated with stirring at 225° C. for 10 min until complete by TLC. The reaction was then transferred directly to a silica gel cartridge and purified by silica gel column chromatography (25 g silica cartridge, 0-3% Et2O/pentane) to yield 2 as a light yellow oil (34 mg, 68%).
Aufarbeitung
- customTo a 2-5 mL MWI vial equipped with a stir bar
- customthe reaction was irradiated
- custompurified by silica gel column chromatography (25 g silica cartridge, 0-3% Et2O/pentane)
Quellen und Nachweise
- ORD-Eintrag
- ord-46db17606a064a7db87efffc7a506bb9
- Quelldatensatz
- uspto-grants-2015_09
- Patentnummer
- US09133234B2
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