Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Phenyl-2-(4-trifluoromethylphenyl)acetonitrile | HCID 23451547 | — |
| Reactant | HCID 178478565 | HCID 178478565 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178510934 | HCID 178510934 | — |
Reaction Steps
A 3.84 g. portion of 2-phenyl-2-(4-trifluoromethylphenyl)acetonitrile was reacted with 1.42 g. of 50% sodium hydride and 2.25 g. of 4-chloromethylimidazole hydrochloride in 50 ml. of dimethylformamide, as described in Example 1. The mixture was stirred for 2 hours at 60° C., and for 20 hours at ambient temperature. The reaction mixture was then worked up as described in Example 1 to obtain 3.6 g. of the desired product as the free base, a sample of which was analyzed as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04281141 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-9790b7df020e4ed9aee7871ee9ba58bc |
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| Source note | uspto-grants-1981_07 |
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