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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133812Erstellt: 26. Oktober 2026

Acetic Acid → Ethyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoate

https://huagongshe.com/reaction/133812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-TetraloneHCID 68266—
EduktEthyl isocyanoacetateHCID 533707—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoateHCID 5973609245%

Reaktionsschritte

To a stirred slurry of potassium t-butoxide (4.7 g, 42.0 mmol) in 30 mL tetrahydrofuran at 0° C. is added ethyl isocyanoacetate (4.53 g, 40.0 mmol). This is stirred for 30 mins whereupon a solution of β-tetralone (5.88 g, 40.0 mmol) in tetrahydrofuran (20 mL) is added dropwise. The reaction mixture is allowed to warm to room temperature and stirred for 3 hours. The reaction mixture is then recooled in an ice bath and to this is added acetic acid (2.5 g, 41.6 mmol), allowed to warm to room temperature and stirred for an additional 30 mins. The solvent is removed in-vacuo and the residue partitioned between water and ethyl acetate. The organic layer is washed with water and brine, dried over sodium sulfate, filtered, evaporated and crystallized from cyclohexane to give 4.67 g of a white solid (contains some E-isomer), MS: m/z 260.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390910B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-a8160e7125b049a2b8a174406f9a3c0f
Quellennotizuspto-grants-2008_06