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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486802Generated: October 28, 2026

Dimethylformamide → N-Methyl-N-(2-(3-chloro-1-methoxyphenyl)ethyl)-1,4-diaminobutane

https://huagongshe.com/reaction/486802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-Bromobutyl)phthalimideHCID 93575—
Reactant2-(3-Chloro-4-methoxyphenyl)ethan-1-amineHCID 2757644—
SolventWaterHCID 962—
ProductN-Methyl-N-(2-(3-chloro-1-methoxyphenyl)ethyl)-1,4-diaminobutaneHCID 6782228747%

Reaction Steps

A mixture comprising 5.00 g of N-methyl-(2-(3-chloro-4-methoxyphenyl)ethylamine, 9.49 g of N-(4-bromobutyl)phthalimide, 4.16 g of anhydrous potassium carbonate and 50 ml of N,N-dimethylformamide was stirred at a room temperature for 14 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate and the ethyl acetate phase was washed with water and a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated, followed by the addition of 50 ml of ethanol and 1.5 ml of hydrazine monohydrate. The obtained mixture was heated under reflux for 2 hours, cooled by allowing to stand and filtered to remove insoluble matter. The filtrate was distilled to obtain 3.16 g of the title compound as a colorless oil (yield: 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292770
Source datasetuspto-grants-1994_03
ORD IDord-ea7447b6929e43bd83d7b0172c2c9739
Source noteuspto-grants-1994_03