HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744524Generated: October 31, 2026
Water → 5-Amino-2-(cyclohexyloxy)benzonitrile
https://huagongshe.com/reaction/1744524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 22227856 | HCID 22227856 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-2-(cyclohexyloxy)benzonitrile | HCID 22228134 | 93.2% |
Reaction Steps
Subsequently, ammonium chloride (1.8 g) and iron powder (9.2 g) were added to a mixed solvent of water (32 ml) and ethanol (130 ml), and the mixture was heated to 65° C. Then, ethanol solution (4 ml) containing 2-cyclohexyloxy-5-nitrobenzonitrile (11.6 g) was added dropwise over 20 min and the mixture was stirred at a refluxing temperature for 30 min. The reaction mixture was ice-cooled and filtrated. The solvent was evaporated under reduced pressure. To the residue was added aqueous sodium hydroxide solution and the mixture was extracted with toluene. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, after which the solvent was evaporated under reduced pressure. n-Hexane was added to the residue to allow crystallization. The crystals were recrystallized from a mixed solvent of diisopropyl ether-n-hexane to give the title compound (9.5 g), melting point: 59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07015218B1 |
|---|
| Source dataset | uspto-grants-2006_03 |
|---|
| ORD ID | ord-ae02e562357742839d9d8993aeab8063 |
|---|
| Source note | uspto-grants-2006_03 |
|---|