HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → N-(4-methoxyphenyl)pyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-methoxyphenyl)pyridin-4-amine | HCID 3628677 | — |
Reaction Steps
A mixture of 1-(4-pyridinium chloride hydrochloride (10.0 g, 0.04 mol) and p-anisidine (4.9 g, 0.04 mol) is heated at 150° C. until the pyridine stops distilling. The resulting black oil is allowed to cool to room temperature during which time it solidifies. The solid is broken into a powder and repeatedly washed with acetone until the color is light brown. Recrystallization from isopropanol gives the product as a yellow powder, mp 129°-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855308 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-b6f1077f4f4d41a0bf24dc5dcf64fa4f |
| Source note | uspto-grants-1989_08 |