HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → 2-Chloro-3-(4-cyano-phenoxy)-6-nitro-N-allyl-aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | 2-Chloro-4-nitro-3-phenoxy-1-(4-cyano-phenoxy)-benzene | HCID 12881153 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-3-(4-cyano-phenoxy)-6-nitro-N-allyl-aniline | HCID 12881165 | — |
Reaction Steps
A mixture of 4 gm of 2-chloro-4-nitro-3-phenoxy-1-(4-cyano-phenoxy)-benzene, 10 ml of dioxane and 2 gm of allylamine was allowed to stand at room temperature for 30 hours. Thereafter, the dioxane was distilled off, the residue was taken up in chloroform, the resulting solution was extracted with dilute sodium hydroxide, the organic phase was dried with sodium sulfate, the chloroform was distilled off, and the residue was recrystallized from ethanol. 3.5 gm (97.2% of theory) of the yellow crystalline title compound, m.p. 85°-87° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04364875 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-c8084c4877234fbeb0017f337ed689db |
| Source note | uspto-grants-1982_12 |