HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269393Generated: October 30, 2026
Bromoacetonitrile → HCID 68958685, compound
https://huagongshe.com/reaction/269393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | HCID 68961430 | HCID 68961430 | — |
| Reactant | HCID 68964281 | HCID 68964281 | — |
| Product | HCID 68958685 | HCID 68958685 | 48% |
| Product | HCID 68964281 | HCID 68964281 | — |
Reaction Steps
5-(3-Pentyl-1-benzofuran-2-yl)-8-hydroxy-quinoline was prepared as a solid (0.113 g, 99%) from 5-(3-pentyl-1-benzofuran-2-yl)-8-methoxy-quinoline according to the procedure described in the first part of Step 4 of Example 2. Mass spectrum (+ESI, [M+H)+) m/z 332. Reaction of 5-(3-Pentyl-1-benzofuran-2-yl)-8-hydroxy-quinoline with bromoacetonitrile according to the procedure described in Step 2 of Example 1 afforded the title compound as a solid (0.059 g, 48%). Mass spectrum (+ESI, [M+H)+) m/z 371. 1H NMR (500 MHz, DMSO-d6): δ 8.94-9.02 (m, 1H), 8.20 (d, 1H, J=9.5 Hz), 7.72-7.83 (m, 2H), 7.60-7.70 (m, 2H), 7.53 (d, 1H, J=8.6 Hz), 7.28-7.42 (m, 2H), 5.52 (s, 2H), 2.68 (t, 2H, J=7.4 Hz), 1.50-1.67 (m, 2H), 1.03-1.26 (m, 4H), and 0.67 ppm (t, 3H, J=7.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446201B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-4986a0f7d85a4196a8e8c6511efd1448 |
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| Source note | uspto-grants-2008_11 |
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