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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250898Generated: October 25, 2026

Ethylamine → N'-(6-Chloro-2-methyl-phenyl)-N-ethyl-propane-1,3-diamine

https://huagongshe.com/reaction/1250898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant1-(6-Chloro-2-methyl-phenyl)amino-3-hydroxy-propaneHCID 18324834—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN'-(6-Chloro-2-methyl-phenyl)-N-ethyl-propane-1,3-diamineHCID 1832482254.3%

Reaction Steps

A mixture of a 2.0 M solution of ethylamine in tetrahydrofuran (139.5 mL) and the hydrobromide salt of Example 12, Step A (9.5 g) was stirred at ambient temperature under nitrogen for 48 hours. The tetrahydrofuran was removed in vacuo and the residue was partitioned between dichloromethane and 1N sodium hydroxide. The extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo to give a brown oil. The crude material was dissolved in dichloromethane and absorbed onto a column of Merck-60 flash silica gel. Elution with a solvent gradient (from 95:5 to 80:20 dichloromethane-methanol containing 0.2% ammonium hydroxide) gave the title compound (3.4 g, 54.3%) as a yellow oil, which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340687B1
Source datasetuspto-grants-2002_01
ORD IDord-87b31028294e4602931608be0f5cbc66
Source noteuspto-grants-2002_01