HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645281Generated: October 30, 2026
6-bromo-1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)one → 1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)-one
https://huagongshe.com/reaction/645281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-bromo-1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)one | HCID 59263436 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)-one | HCID 59263414 | 97% |
Reaction Steps
A mixture of 6-bromo-1′-pentylspiro[1-benzofuran-3,3′-indol]-2′(1′H)-one (0.10 g, 0.27 mmol) and palladium/carbon (0.09 g, 0.01 mmol) in methanol/ethyl acetate (1/1, 4.00 mL) was stirred under hydrogen at atmospheric pressure for 16 h. The solvent was evaporated and the black residue was subjected to column chromatography (ethyl acetate/hexane, 1/6) to give the title compound (0.08 g, 97%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.30 (dd, 1H), 7.18 (dd, 1H), 7.20 (d, 1H), 7.02 (dd, 1H), 6.96-6.90 (m, 2H), 6.79 (dd, 1H), 6.69 (d, 1H), 4.93 (d, 1H), 4.67 (d, 1H), 3.89-3.64 (m, 2H), 1.81-1.66 (m, 2H), 1.44-1.31 (m, 4H), 0.92 (t, 3H); 13C NMR (75 MHz, CDCl3) δ 177.2, 160.7, 142.5, 132.8, 129.7, 129.0, 128.8, 123.9, 123.3, 123.1, 121.3, 110.4, 108.6, 58.1, 40.4, 29.0, 27.2, 22.3, 14.0; MS (ES+) m/z 308.5 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700641B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-3c798a1ca2e14d4896312112d57a64a5 |
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| Source note | uspto-grants-2010_04 |
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