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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902594Generated: November 3, 2026

Benzylamine → 2-Chloro-3-(2,5-dichloro-4-methylthio-phenoxy)-6-nitro-N-benzyl-aniline

https://huagongshe.com/reaction/1902594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant2-Chloro-4-nitro-3-phenoxy-1-(2,5-dichloro-4-methylthio-phenoxy)-benzeneHCID 70545315—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3-(2,5-dichloro-4-methylthio-phenoxy)-6-nitro-N-benzyl-anilineHCID 7054329588.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 4.6 gm of 2-chloro-4-nitro-3-phenoxy-1-(2,5-dichloro-4-methylthio-phenoxy)-benzene, 3.0 gm of benzylamine and 10 ml of dioxane was stirred for 6 hours at 40° C. Thereafter, the reaction mixture was allowed to stand overnight and was then evaporated. The residue was taken up in chloroform, and the resulting solution was extracted first with dilute sodium hydroxide and then with water, dried with sodium sulfate and evaporated. The dark brown oil left behind was purified on a silicagel column, yielding 4.2 gm of the thin-layer chromatographically uniform title compound in the form of an orange, viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364875
Source datasetuspto-grants-1982_12
ORD IDord-7bf46ab9ebb34437b1cb25bcc909c1a5
Source noteuspto-grants-1982_12