Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Chlorophenyl)phenylacetonitrile | HCID 4414244 | — |
| Reactant | HCID 178478565 | HCID 178478565 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178510935 | HCID 178510935 | — |
Reaction Steps
As described in Example 1, 2.04 g. of 50% sodium hydride, 10.12 g. of 2-(4-chlorophenyl)-2-phenylacetonitrile, and 3.06 g. of 4-chloromethylimidazole hydrochloride were reacted in 50 ml. of dimethylformamide. The reaction mixture was stirred for one hour at 60° C. and then for 20 hours at ambient temperature. Evaporation of the solvent and work up as described in Example 1 produced 5.3 g. of the product named above, which was converted to the maleate salt and crystallized from acetone/diethyl ether to obtain 6.29 g. of the maleate salt of the desired product, m.p. 135°-136° C.
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-e1c8a855b2c3480eb59c38d4b7d75d57 |
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| Source note | uspto-grants-1981_07 |
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