Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Benzofuranacetonitrile | HCID 12600735 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54066355 | HCID 54066355 | 42.6% |
Reaction Steps
2-Iodopropane (6.5 g, 0.038 mol) was added to a well-stirred mixture of benzofuran-6-acetonitrile (3.0 g, 0.019 mol), tetrabutylammonium hydrogen sulphate (6.5 g, 0.019 mol), sodium hydroxide (47% w/w, 20 cm3, 0.037 mol), water (10 cm3) and dichloromethane (50 cm3), and the mixture was refluxed for 6 hr. with good stirring. The organic layer was washed with water, dried (Na2SO4), filtered and the solvent was removed. Toluene (15 cm3) was added to the residue, the mixture was filtered, and the solvent was removed. The residue was chromatographed on silica using toluene as eluant, to give α-isopropylbenzofuran-6-acetonitrile (1.62, 0.0081 mol, 42.6%) as an oil. (Found: C, 79.32; H, 6.22; N, 6.55. C13H13NO requires C, 78.36, H, 6.58; N, 7.03%) t.l.c./silica/toluene RF 0.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04372970 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-0dfbde7671db48dbb59306d752066a6f |
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| Source note | uspto-grants-1983_02 |
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