HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Hydroxydiphenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Hydroxydiphenylamine | HCID 31208 | 27.4% |
Reaction Steps
0.93 g of aniline, 2.24 g of 1,4-cyclohexanedione and 1.4 ml of triethylamine were heated with stirring in 15 ml of ethanol at 50° C. to 60° C. and reacted in air for 8 hours. During the reaction, ethanol was added as needed. After concentrating the reaction mixture under reduced pressure, the resultant was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) and 0.50 g of N-(4-hydroxyphenyl)aniline was obtained (yield 27.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750156B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-44dc6663f00845ad8160334a997c3594 |
| Source note | uspto-grants-2010_07 |