Hydrochloric Acid → 4,4-Diethoxy-1-(4-nitrophenyl)but-2-yn-1-one

HRID 456791

Reaktionsgleichung

[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[C:5]#[CH:6])[CH3:2].[Li]CCCC.CON(C)[C:18](=[O:28])[C:19]1[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=1.Cl>C1COCC1>[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[C:5]#[C:6][C:18]([C:19]1[CH:20]=[CH:21][C:22]([N+:25]([O-:27])=[O:26])=[CH:23][CH:24]=1)=[O:28])[CH3:2]

Komponenten

Reaktionsbedingungen

Temperatur: -70 °C

Versuchsvorschrift

3,3-Diethoxyprop-1-yne (8.5 ml, 59 mmol) was dissolved in THF (100 ml). The solution was cooled to −70° C., and nBuLi (19 ml of 2.5 M soln in hexanes, 47.5 mmol) was added over 5 min. The solution was warmed to 0° C. for 15 min, then cooled to −70 ° C. again. A solution of N-methoxy-N-methyl-4-nitrobenzamide (Intermediate 8, 8.04 g, 38.1 mmol) in THF (50 ml) was added dropwise over 15 min. The solution was warmed to 0° C. after 15 min, and held there for 45 min. The reaction mixture was poured into 1M HCl, extracted with ethyl acetate and dried over sodium sulfate. Purification by chromatography on silica gel eluting with 30 to 50% dichloromethane: hexane, gave the title compound as a light orange oil which solidified on standing (7.14 g).

Aufarbeitung

temperatureThe solution was warmed to 0° C. for 15 min
temperaturecooled to −70 ° C. again
temperatureThe solution was warmed to 0° C. after 15 min
extractionextracted with ethyl acetate
dry with materialdried over sodium sulfate
customPurification by chromatography on silica gel eluting with 30 to 50% dichloromethane

Quellen und Nachweise

ORD-Eintrag: ord-52ad3e59f4f24aa3a7736f9b578531f6
Quelldatensatz: uspto-grants-2007_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07186738B2

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