Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1463925Erstellt: 26. Oktober 2026

Tetrahydrofuran → morpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide

https://huagongshe.com/reaction/1463925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt4-AcetylmorpholineHCID 15543—
EduktLithium diisopropylamideHCID 2724682—
EduktMethyl-2-benzyloxyphenyl propiolateHCID 54058410—
LösungsmittelWaterHCID 962—
Produktmorpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamideHCID 8674728661%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Acetyl morpholine (546 ul, 4.72 mmole) was dissolved in 10 ml dry tetrahydrofuran in an oven dried 50 ml two neck round bottom flask under nitrogen. The solution was cooled to 0° C. and was treated slowly dropwise with lithium diisopropylamide (3.2 ml, 4.72 mmole). The mixture was stirred 30 minutes at 0° C. and was treated with methyl-2-benzyloxyphenyl propiolate (600 mg, 2.25 mmole) in 2 ml dry tetrahydrofuran. The reaction mixture was stirred for 1 hour at 0° C. and was diluted with 10 ml water. The volatiles were removed in vacuo and the residue was crystallized from diethyl ether/methanol (20:1). The tan solid was collected, was washed with diethyl ether, and was dried to afford 500 mg (61%) of morpholine-5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide as a tan solid. Melting Point: 224°-227° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05302613
Quelldatensatzuspto-grants-1994_04
ORD IDord-c351075d065040a1ba1d312e4d965ae0
Quellennotizuspto-grants-1994_04