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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902596Generated: November 2, 2026

4-Chlorobenzylamine → 2-Chloro-3-phenoxy-6-nitro-N-(4-chloro-benzyl)-aniline

https://huagongshe.com/reaction/1902596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
Reactant2-Chloro-4-nitro-1,3-diphenoxy-benzeneHCID 12881147—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3-phenoxy-6-nitro-N-(4-chloro-benzyl)-anilineHCID 12881162—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5 gm of 2-chloro-4-nitro-1,3-diphenoxy-benzene, 10 ml of dioxane and 6 gm of 4-chlorobenzylamine was stirred for 12 hours at 80° C. Thereafter, the reaction mixture was evaporated, the residue was taken up in chloroform, the resulting solution was extracted with 1 N sodium hydroxide, and the organic phase was dried with sodium sulfate. The chloroform was distilled off, and the residue was recrystallized from ethanol, yielding 4.7 gm (82.7% of theory) of the title compound, m.p. 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364875
Source datasetuspto-grants-1982_12
ORD IDord-95f192373adf4dd7a632ed674995a2da
Source noteuspto-grants-1982_12