Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Trifluoromethyl)phenylacetonitrile | HCID 75359 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Product | HCID 21181229 | HCID 21181229 | 64.4% |
Reaction Steps
To a mixture of 4-trifluoromethyl-phenylacetonitrile (5.00 g, 27.0 mmoles), 50% aqueous sodium hydroxide solution (1.9 g), sodium hydroxide (270 mg), and tetra n-butylammonium chloride (1.2 g) stirring in a 60° oil bath was added 2-bromopropane (3.32 g, 27.0 mmoles). The resulting mixture was stirred at 80° for 0.5 hours, and then at 90-95° for 1.0 hours longer. After cooling, the mixture was partitioned between toluene and water. The organic layer was washed with water, dried over anhydrous sodium sulfate, filtered and then evaporated. Chromatography of the residue over silica gel using 10% ethyl acetate-hexane as eluent gave the title compound (3.95 g) as an orange oil which was characterized by NMR as follows: 1H NMR (CDCl3) d 7.67(d, 2H), 7.48(d, 2H), 3.77(d, 1H), 2.18(m, 1H), 1.13(d, 3H), 1.06(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-9fcf1b51cbe049f19412326fbcd558b1 |
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| Source note | uspto-grants-2001_07 |
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