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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869850Generated: October 26, 2026

1-(Benzofuran-5-yl)cyclopropanecarboxylic acid → 1-(2,3-Dihydrobenzofuran-5-yl)cyclopropanecarboxylic acid

https://huagongshe.com/reaction/869850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzofuran-5-yl)cyclopropanecarboxylic acidHCID 51358454—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
Product1-(2,3-Dihydrobenzofuran-5-yl)cyclopropanecarboxylic acidHCID 5135845547%

Reaction Steps

To a solution of 1-(benzofuran-5-yl)cyclopropanecarboxylic acid (700 mg, 3.47 mmol) in MeOH (10 mL) was added PtO2 (140 mg, 20%) at room temperature. The stirred reaction mixture was hydrogenated under hydrogen (1 atm) at 10° C. for 3 days. The reaction mixture was filtered. The solvent was evaporated under vacuum to afford the crude product, which was purified by preparative HPLC to give 1-(2,3-dihydrobenzofuran-5-yl)cyclopropanecarboxylic acid (330 mg, 47%). 1H NMR (400 MHz, CDCl3) δ 7.20 (s, 1H), 7.10 (d, J=10.8 Hz, 1H), 6.73 (d, J=11.2 Hz, 1H), 4.57 (t, J=11.6 Hz, 2H), 3.20 (t, J=11.6 Hz, 2H), 1.67-1.63 (m, 2H), 1.25-1.21 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-5dc5bab9ac384aa7a6dc379aa9764408
Source noteuspto-grants-2015_03