Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377708Generated: October 25, 2026

Triethylamine → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2-furancarboxamido)propyloxy)-benzene

https://huagongshe.com/reaction/377708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-[2,6-Dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propylamineHCID 15869744—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2-furancarboxamido)propyloxy)-benzeneHCID 2200677167.9%

Reaction Steps

To a mixture of 0.35 g of 4-(3-aminopropyloxy)-3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)benzene, 0.19 g of 5-bromo-2-furancarboxylic acid, 0.18 ml of triethylamine and 10 ml of chloroform was added 0.23 g of WSC hydrochloride, while stirring at room temperature. After stirring at room temperature for 6 hours, the reaction mixture was concentrated to give a residue. The residue was dissolved in 50 ml of ethyl acetate, and the ethyl acetate layer was successively washed with 10% hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated to give a residue. The residue was subjected to silica gel chromatography, which afforded 0.35 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2 -furancarboxamido)propyloxy)benzene (64% yield), nD24.0 1.5918.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028100
Source datasetuspto-grants-2000_02
ORD IDord-90fd8e9d3e7d48c5bc03484c0e6da5bf
Source noteuspto-grants-2000_02