HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamide → N-[3-(4-aminophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamide | HCID 57386826 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(4-aminophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide | HCID 57386827 | 98% |
Reaction Steps
To a solution of 3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamide (8.10 g, 20.2 mmol) in tetrahydrofuran (50 mL) and methanol (50 mL) was added 10% palladium-carbon (555 mg), and the mixture was stirred under a hydrogen atmosphere (2.5 atm) at room temperature for 14 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (7.34 g, 98%) as a pale-gray amorphous substance. The obtained compound was used in the next reaction without a further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324395B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-2e08fdc4a94f463d8bcdccd551979ead |
| Source note | uspto-grants-2012_12 |