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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902595Generated: November 1, 2026

Allylamine → HCID 12881159, compound

https://huagongshe.com/reaction/1902595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantHCID 12881150HCID 12881150—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 12881159HCID 12881159—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 4.9 gm of 2-chloro-4-nitro-5-phenoxy-1-(2,5-dichloro-4-bromo-phenoxy)-benzene, 1.8 gm of allylamine and 10 ml of dioxane was stirred first for 7 hours at 40° C. and then for 3 hours at 60° C. Thereafter, the reaction solution was evaporated, the residue was taken up in chloroform, and the resulting solution was washed first with an acid solution and then with an alkaline solution, dried with sodium sulfate and evaporated. The raw reaction product thus obtained (5.6 gm) was purified on a silicagel column, yielding 3.0 gm (66.6% of theory) of the yellow crystalline title compound, m.p. 102.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364875
Source datasetuspto-grants-1982_12
ORD IDord-1f193b4b21864f67bf456f58dda88684
Source noteuspto-grants-1982_12