HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodophenylacetonitrile → N-p-Benzeneacetonitrile menthanecarboxamide, (+)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodophenylacetonitrile | HCID 142866 | — |
| Reactant | N-p-Benzeneacetonitrile menthanecarboxamide | HCID 44467796 | — |
| Reactant | (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide | HCID 59253418 | — |
| Product | N-p-Benzeneacetonitrile menthanecarboxamide, (+)- | HCID 46174464 | — |
Reaction Steps
N-[4-(cyanomethyl)phenyl]-(1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide was prepared as described above for the preparation of the N-[4-(cyanomethyl)phenyl]-(1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide isomer, i.e., by coupling the (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide prepared in steps A to C above with 4-(cyanomethyl)phenyl iodide. The (1S,2S,5R)-material (neoisomer) has the following properties with structure confirmed by obtaining an X-ray crystal structure of a sample crystallized from hexane/ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754259B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-dfbe441642734b90ab4929d3eee94f83 |
| Source note | uspto-grants-2014_06 |