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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662466Generated: October 26, 2026

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

https://huagongshe.com/reaction/1662466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentane, methylene-HCID 73714—
ReactantMethyl 4-(allyloxy)benzoateHCID 4645407—
Catalyst(1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)rutheniumHCID 11763533—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(2-cyclopentylideneethoxy)benzoateHCID 5746765268%

Reaction Conditions

Temperature55 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-6bdae972316d4ef39d8fa7e3e551bd8d
Source noteuspto-grants-2011_10