HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzofuran-5-yl)cyclopropanecarboxylic acid → 1-(2,3-Dihydrobenzofuran-5-yl)cyclopropanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzofuran-5-yl)cyclopropanecarboxylic acid | HCID 51358454 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2,3-Dihydrobenzofuran-5-yl)cyclopropanecarboxylic acid | HCID 51358455 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741321B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-d1b05cf923a64270814be2ccfc773e4f |
| Source note | uspto-grants-2010_06 |