HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → N-(4-Hydroxyphenyl)nonadecanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Nonadecanoyl chloride | HCID 4250939 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-(4-Hydroxyphenyl)nonadecanamide | HCID 19597124 | 83% |
Reaction Steps
Under a nitrogen atmosphere, p-aminophenol (109 g) was suspended in methyl ethyl ketone (2000 ml). To this suspension was added triethylamine (253 g) and then was added nonadecanoyl chloride (331 g), followed by refluxing with heating for 2 hours. The reaction mixture was cooled to room temperature to precipitate a white crystal. This crystal was filtered off under reduced pressure and recrystallized from methyl ethyl ketone to obtain 323 g of the desired product. Yield 80%; m.p. 138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05395815 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-ae9c97feff854c1e9a6833c67b6000ce |
| Source note | uspto-grants-1995_03 |