HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 3432930, compound → 2-(2-Chlorophenoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 3432930 | HCID 3432930 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Chlorophenoxy)aniline | HCID 12569012 | — |
Reaction Steps
A solution of 2-chloro-(2-nitrophenoxy)benzene (5.00 g) in tetrahydrofuran (100 mL) was shaken in a Parr Hydrogenator over Raney nickel at 5 psi hydrogen at room temperature for 4 hours. The catalyst was filtered from the reaction, and the solution was evaporated under vacuum to a yellowish oil which crystallized on standing. The solid was crushed, suspended in hexane and filtered to yield the title compound as a light orange solid. Mp: 44°-45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05461046 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-6ffd3e060b3c4617a49ca880d5b13ca5 |
| Source note | uspto-grants-1995_10 |