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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentane, methylene- | HCID 73714 | — |
| Reactant | Methyl 4-(allyloxy)benzoate | HCID 4645407 | — |
| Catalyst | (1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)ruthenium | HCID 11763533 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(2-cyclopentylideneethoxy)benzoate | HCID 57467652 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-6bdae972316d4ef39d8fa7e3e551bd8d |
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| Source note | uspto-grants-2011_10 |
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