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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 657164Erstellt: 25. Oktober 2026

Ethyl formate → HCID 178517727, Verbindung

https://huagongshe.com/reaction/657164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl formateHCID 8025—
EduktSodium hydrideHCID 24758—
Eduktethyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetateHCID 10899396—
EduktCinnamimidamideHCID 14668188—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthanol, mixt. with methanolHCID 18681192—
ProduktHCID 178517727HCID 17851772763,2%

Reaktionsschritte

NaH (0.38 g, 9.5 mmol, 60% paraffin oil) was added slowly to a THF (20 mL) solution of ethyl (tetrahydro-2H-pyran-2-yloxy)acetate (prepared by treating ethyl hydroxyacetate with 3,4-dihydro-2H-pyran and TsOH) (1.0 g, 5.3 mmol) and dry ethyl formate (3.9 g, 53 mmol). The reaction mixture was stirred at room temperature for 15 min. and then heated at 65° C. for 45 min. The reaction mixture was concentrated to dryness to give a pale yellow solid. The solid was added to a MeOH/EtOH (20 mL/20 mL) solution of (2E)-3-phenyl-2-propenimidamide (0.78 g, 5.3 mmol), the subsequent mixture was heated at 80° C. for 4 h. The resulting material was poured into DCM (10 mL) containing silica gel (3 g) and evaporated. Purification by column chromatography (silica gel) using a MeOH/DCM gradient (0-10%) provided the desired product as a pale yellow solid (1 g, 63%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071592B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-6879b79ccf234b85af1804df33b3675c
Quellennotizuspto-grants-2011_12