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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6398Erstellt: 23. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 3-oxo-4-phenyl-2-(1-cyano-6-methoxy-1,2,3,4-tetrahydronaphth-2-yl)-butyrate

https://huagongshe.com/de/reaction/6398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktMethyl 3-oxo-4-phenylbutanoateHCID 2760261—
Edukt1-Naphthalenecarbonitrile, 3,4-dihydro-6-methoxy-HCID 3014466—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 3-oxo-4-phenyl-2-(1-cyano-6-methoxy-1,2,3,4-tetrahydronaphth-2-yl)-butyrateHCID 1979328165%

Reaktionsschritte

Methyl 3-oxo-4-phenylbutyrate (29.33 g, 153 mmol) and 1-cyano-6-methoxy-3,4-dihydronaphthalene (25.7, 139 mmol), the product of Step 2 of Example 1, were dissolved in 25 mL of acetonitrile. DBU (1.5 mL) was added and the reaction mixture was stirred for 2 h at ambient temperature. A second aliquot of DBU (1.5 mL) was then added and stirring continued overnight. The reaction mixture was partitioned between diethyl ether and 1N aqueous hydrochloric acid solution (4:1) and the aqueous layer was extracted with diethyl ether. The combined organic layers were washed with 1N aqueous hydrochloric acid and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on silica gel eluted with hexane/ethyl acetate (6:1) to give 33.9 g (65% yield) of the title compound; MS DCl--NH3M/Z: 395 (M+NH4)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05248677
Quelldatensatzuspto-grants-1993_09
ORD IDord-4f061f4471424f05a5f309faf9ef5632
Quellennotizuspto-grants-1993_09