HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethyl-4-nitroaniline → 2-[(2,6-Dimethyl-4-nitrophenyl)amino]-1-pyrroline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethyl-4-nitroaniline | HCID 28159 | — |
| Reactant | 2-Chloro-1-pyrroline | HCID 13520141 | — |
| Product | 2-[(2,6-Dimethyl-4-nitrophenyl)amino]-1-pyrroline | HCID 20272394 | — |
Reaction Steps
A mixture of 2-chloro-1-pyrroline, prepared as in Example 1, and 19.9 g (0.12 mole) of the aniline product of Example 6 were heated at reflux overnight, according to the general method of Example 8. The title compound was isolated and used for subsequent reactions without further purification. Structure assignment was supported by nmr and infrared spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04533739 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-b73808b27f264206b52ae5c5d7b1945f |
| Source note | uspto-grants-1985_08 |