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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | 2-Chloro-4-nitro-1,3-diphenoxy-benzene | HCID 12881147 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-3-phenoxy-6-nitro-N-(4-chloro-benzyl)-aniline | HCID 12881162 | — |
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
| 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-95f192373adf4dd7a632ed674995a2da |
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| Source note | uspto-grants-1982_12 |
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