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HRID 1662466Erstellt: 24. Oktober 2026

Cyclopentane, methylene- → Methyl 4-(2-cyclopentylideneethoxy)benzoate

https://huagongshe.com/de/reaction/1662466

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopentane, methylene-HCID 73714—
EduktMethyl 4-(allyloxy)benzoateHCID 4645407—
Katalysator(1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)rutheniumHCID 11763533—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-(2-cyclopentylideneethoxy)benzoateHCID 5746765268%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a solution of methyl 4-(allyloxy)benzoate 66.67A (3.00 g, 16.0 mmol) and methylenecyclopentane (1.9 g, 23.0 mmol) in DCM (5.0 mL) was added Hoveyda Grubbs reagent (0.39 g, 0.62 mmol) at room temperature. The resulting reaction mixture was degassed three times and stirred at 55° C. under nitrogen overnight. The reaction mixture was purified by Combi Flash silica gel chromatography (hexane/EtOAc 95/5) to give the compound 66.67B, (2.60 g, yield 68%). 1H NMR (500 MHz, CDCl3) δ ppm 7.82-7.93 (2H, m), 6.80-6.88 (2H, m), 5.44-5.56 (1H, m), 4.47 (2H, d, J=6.6 Hz), 3.80 (3H, s), 2.20-2.31 (4H, m), 1.50-1.71 (4H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030354B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-6bdae972316d4ef39d8fa7e3e551bd8d
Quellennotizuspto-grants-2011_10