Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2,6-Difluorophenyl)acetonitrile | HCID 69559 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | HCID 21181206 | HCID 21181206 | 75.5% |
Reaction Steps
A mixture of 2,6-difluorophenylacetonitrile (10.0 g, 65.4 mmoles), 50% aqueous sodium hydroxide (4.6 g), sodium hydroxide (653 mg), tetra-n-butylammonium bromide (2.90 g and 2-bromopropane (8.85 g, 71.9 mmoles) was stirred while heating to 80-85 over 1.0 hours, and then maintained at that temperature for 2.0 hours. After cooling, the mixture was partitioned between diethyl ether and water, the aqueous layer extracted with ether and the combined organic extracts washed with brine, dried over magnesium sulfate, filtered and the solvent evaporated. The residue was distilled to give a product compound (9.64 g) as a water-white liquid, b.p. 92-94° (3 mm) which was characterized by NMR as follows: 11H NMR(CDCl)3 d 7.32(m, 1H), 6.95(m, 2H), 3.84(d, 1H), 2.32(m, 1H), 1.24(d, 3H), 0.89(d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265439B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-4ec4e3565b534dbfab10b5accaed4475 |
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| Source note | uspto-grants-2001_07 |
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