Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p,p'-Ddcn | HCID 8806 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178478565 | HCID 178478565 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178510939 | HCID 178510939 | — |
Reaction Steps
As described in Example 1, 7.26 g. of 2,2-bis(4-chlorophenyl)acetonitrile, 1.33 g. of 50% sodium hydride and 2.12 g. of 4-chloromethylimidazole hydrochloride were reacted in 50 ml. of dimethylformamide. The mixture was stirred for 2 hours at 60° C. and then 21 hours at ambient temperature. The solvent was then evaporated off under vacuum and the reaction mixture was worked up as described in Example 1 to obtain 5.2 g. of the free base named above, which was converted to the maleate salt and crystallized from acetone/diethyl ether to obtain 5.73 g. of the maleate salt of the product named above, m.p. 151.5°-153° 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-37b27b6dc4ec4f3f94789648c81585dd |
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| Source note | uspto-grants-1981_07 |
|---|