HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Isothiocyanate → (cyclohexylphenylamino)-N-benzylthiocarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Isothiocyanate | HCID 2346 | — |
| Reactant | N-Cyclohexylaniline | HCID 74567 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (cyclohexylphenylamino)-N-benzylthiocarboxamide | HCID 21304109 | — |
Reaction Steps
To a solution of N-cyclohexylaniline (0.1 ml, 0.57 mmol) in acetonitrile (4 ml) was added a catalytic amount of 4-(dimethylamino)pyridine (5 mg, 0.04 mmol). To this mixture was added benzyl isothiocyanate (0.11 ml, 0.83 mmol) dropwise, and the mixture was stirred at room temperature for 16 hours. The solvent was removed under reduced pressure, and the residue purified on preparative silica gel plates, developing with 20% ethyl acetate/hexanes, to furnish (cyclohexylphenylamino)-N-benzylthiocarboxamide as a white solid, (M+1)=324.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713650B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-b72946b816d94e4e912db09fc4cec590 |
| Source note | uspto-grants-2004_03 |