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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970195Generated: October 31, 2026

4-Iodophenylacetonitrile → N-p-Benzeneacetonitrile menthanecarboxamide, (+)-

https://huagongshe.com/reaction/1970195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenylacetonitrileHCID 142866—
ReactantN-p-Benzeneacetonitrile menthanecarboxamideHCID 44467796—
Reactant(1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamideHCID 59253418—
ProductN-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426643B2
Source datasetuspto-grants-2013_04
ORD IDord-fc29fdb7491f40b4b4e46192cf8c6e57
Source noteuspto-grants-2013_04