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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353071Generated: October 30, 2026

4-[2-Methoxyethenyl]-1-phenylbicyclo[2.2.2]octane → Methyl (4-phenylbicyclo[2.2.2]oct-1-yl)acetate

https://huagongshe.com/reaction/2353071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[2-Methoxyethenyl]-1-phenylbicyclo[2.2.2]octaneHCID 67414504—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductMethyl (4-phenylbicyclo[2.2.2]oct-1-yl)acetateHCID 2501642759%

Reaction Steps

To a stirred solution of 4-[2-methoxyethenyl]-1-phenylbicyclo[2.2.2]octane (Intermediate 7; 12.6 g, 51.99 mmol) in DCM (200 mL) was added pyridinium chlorochromate (33.6 g, 155.97 mmol) in portions and the reaction mixture was allowed to stir at ambient temperature for 2 hrs. Further pyridinium chlorochromate (12 g, 55.99 mmol) was added and stirring was continued for a further 1 hr. The mixture was filtered and the filtrate was concentrated under reduced pressure, ether (200 mL) was added and the organic phase was washed with water (200 mL). Water (200 mL) and ether (2×200 mL) were added to the filtered solid and the mixture was filtered through a pad of celite. The organic extracts were combined, dried (MgSO4) and concentrated to leave a brown gum. This was purified on a 330 g Crawford silica cartridge, loading the sample in DCM and eluting with 5-10-20% EtOAc-isohexane to provide the title compound as a cream solid (7.89 g, 30.53 mmol, 59%); 1H NMR (CDCl3) δ 1.63-1.71 (6H, m), 1.83-1.93 (6H, m), 2.17 (2H, s), 3.67 (3H, s), 7.14-7.19 (1H, m), 7.29-7.32 (4H, m); GC-MS EI m/e M+ 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749997B2
Source datasetuspto-grants-2010_07
ORD IDord-fe704a462d104d88a1b06ce1f5ccd05c
Source noteuspto-grants-2010_07