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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605511Generated: November 3, 2026

Acetic Acid → 3-[4-(Methoxycarbonyl)bicyclo[2.2.2]oct-1-yl]propanoic acid

https://huagongshe.com/reaction/605511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantmethyl 4-[(1E)-3-(benzyloxy)-3-oxoprop-1-en-1-yl]bicyclo[2.2.2]octane-1-carboxylateHCID 22591724—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product3-[4-(Methoxycarbonyl)bicyclo[2.2.2]oct-1-yl]propanoic acidHCID 22591703—

Reaction Steps

Diester 2-2 (0.625 g, 1.90 mmol) was dissolved in a 1:1 mixture of ethyl acetate/methanol (30 mL), placed under nitrogen atmosphere, then treated with 10% Pd/C (500 mg) and 0.1 mL of acetic acid. The reaction was placed under hydrogen atmosphere and stirred vigorously for 2 hr. The resulting solution was filtered through celite and the solvent was removed under reduced pressure. The residue was partitioned between 200 mL of ethyl acetate and 200 mL of 1 N NaOH solution. The aqueous layer was separated and neutralized, then extracted three times with 50 mL of methylene chloride. The combined organic layers were dried over magnesium sulfate and the solvent was removed under reduced pressure to afford 3-[4-(methoxycarbonyl)bicyclo[2.2.2]oct-1-yl]propanoic acid (2-3). 1H NMR (500 MHz, CDCl3): δ 3.62 (3H, s), 2.20 (2H, broad t, J=9 Hz), 1.75 (6H, m), 1.47 (2H, broad t, J=9 Hz), 1.38 (6H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915252B2
Source datasetuspto-grants-2011_03
ORD IDord-4d7064974d804828a919a6b9f8aad988
Source noteuspto-grants-2011_03