HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359235Generated: November 2, 2026
Tin tetrachloride → 2-{[1-Chloro-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}acetonitrile
https://huagongshe.com/reaction/1359235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | 2-{[6-(1-Benzofuran-2-yl)-1-chloro-2-naphthyl]oxy}acetonitrile | HCID 18182813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[1-Chloro-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}acetonitrile | HCID 18182795 | — |
Reaction Steps
Following the procedure described in Step 3 of Example 23, 2-{[6-(1-benzofuran-2-yl)-1-chloro-2-naphthyl]oxy}acetonitrile (6.12 g, 18.3 mmol) was acylated with valeryl chloride (2.2 mL, 19 mmol) in presence of tin (IV) chloride (2.2 mL, 19 mmol) in methylene chloride (37 mL). Purification by HPLC using 20% ethyl acetate in hexane as the mobile phase yielded 2-{[1-chloro-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}acetonitrile as a yellow waxy solid (2.55 g), mp 86-89° C. Mass spectrum (+ESI, [M+H]+) m/z 418. 1HNMR (500 MHz, DMSO-d6): δ8.55 (d, 1H, J=1.4 Hz), 8.3 (d, 1H, J=8.9 Hz), 8.25 (d, 1H, J=9.2 Hz), 8.0-8.05 (m, 2H), 7.75-7.8 (m, 2H), 7.4-7.5 (m, 2H), 5.5 (s, 2H), 2.75 (t, 2H, J=7.3 Hz), 1.5-1.6 (m, 2H), 1.1-1.2 (m, 2H), and 0.75 ppm (t, 3H, J=7.4 Hz). Elemental Analysis for C12H20ClNO3: Calculated: C, 71.85; H, 4.82; N, 3.35. Found: C, 71.73; H, 4.59; N, 3.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599925B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-1c1ce0e8cae74322a8c015b734b5ff5f |
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| Source note | uspto-grants-2003_07 |
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