Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902599Generated: November 1, 2026

Allylamine → 2-Chloro-3-(4-cyano-phenoxy)-6-nitro-N-allyl-aniline

https://huagongshe.com/reaction/1902599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
Reactant2-Chloro-4-nitro-3-phenoxy-1-(4-cyano-phenoxy)-benzeneHCID 12881153—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3-(4-cyano-phenoxy)-6-nitro-N-allyl-anilineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364875
Source datasetuspto-grants-1982_12
ORD IDord-c8084c4877234fbeb0017f337ed689db
Source noteuspto-grants-1982_12