HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Chlorophenoxy)aniline → HCID 68705038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Chlorophenoxy)aniline | HCID 7578 | — |
| Reactant | 3-Benzyloxybenzaldehyde | HCID 74342 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68705038 | HCID 68705038 | 67.3% |
Reaction Steps
Reference to α-amino nitrile synthesis: Synlett, 2005, 8, 1325. A methanol solution (50 mL) of 3-benzyloxybenzaldehyde (5 g, 23.6 mmol), 4-amino-4-chlorodiphenyl ether (5.7 g, 25.9 mmol), iodine (120 mg, 0.47 mmol) and trimethylsilylcyanide (3.8 mL, 28.3 mmol) is stirred at room temperature for 18 h. The precipitate that formed is collected and rinsed with ethyl acetate/hexane (1:4) to obtain ˜7 g (67%) of 2-(4-(4-chlorophenoxy)phenylamino)-2-(3-(benzyloxy)phenyl)acetonitrile as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431607B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-0afec78f78d74b47b54f3d56cffa7041 |
| Source note | uspto-grants-2013_04 |