Water → (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran

HRID 234255

Reaktionsgleichung

[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[CH2:7]([Li])CCC.[C:12]([NH:15][C:16]1[C:17]([CH3:30])=[C:18]([CH3:29])[C:19]2[O:23][C:22]([CH:25]=O)([CH3:24])[CH2:21][C:20]=2[C:27]=1[CH3:28])(=[O:14])[CH3:13].O>[Cl-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1>[C:12]([NH:15][C:16]1[C:17]([CH3:30])=[C:18]([CH3:29])[C:19]2[O:23][C:22]([CH3:24])(/[CH:25]=[CH:7]\[C:3]3[CH:2]=[CH:1][CH:6]=[CH:5][CH:4]=3)[CH2:21][C:20]=2[C:27]=1[CH3:28])(=[O:14])[CH3:13]

Komponenten

Reaktionsbedingungen

Temperatur: -20 °C

Versuchsvorschrift

A suspension of benzyltriphenylphosphonium chloride (0.7 g, 1.8 mmol) in tetrahydrofuran (10 ml) was cooled to -20° C. and n-butyllithium hexane solution (1.6M, 1.12 ml, 1.8 mmol) was added dropwise. The reaction mixture was stirred for 30 minutes and then a solution of 5-acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (0.45 g, 1.7 mmol) in tetrahydrofuran (5 ml) was added. The reaction mixture was stirred at room temperature for additional 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extract was washed with water, dried and then concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1) to obtain the desired compound (0.44 g, yield: 76.2%) as oil.

Aufarbeitung

stirringThe reaction mixture was stirred at room temperature for additional 30 minutes
extractionthe product was extracted with ethyl acetate
washThe extract was washed with water
customdried
concentrationconcentrated
customThe residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1)

Quellen und Nachweise

ORD-Eintrag: ord-58df597f495940dda9f2b60e6efab7b3
Quelldatensatz: uspto-grants-1997_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05594154

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