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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-Chloro-4-nitro-3-phenoxy-1-(2,5-dichloro-4-methylthio-phenoxy)-benzene | HCID 70545315 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-3-(2,5-dichloro-4-methylthio-phenoxy)-6-nitro-N-benzyl-aniline | HCID 70543295 | 88.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04364875 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-7bf46ab9ebb34437b1cb25bcc909c1a5 |
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| Source note | uspto-grants-1982_12 |
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