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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64925Generated: October 25, 2026

Triethylamine → 2-[beta-(2-furyl)acrylamido]-N5-methyl-N1,N1-di(n-propyl)pentane-1,5-diamide

https://huagongshe.com/reaction/64925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantFurylacrylic acidHCID 10876—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 86740989HCID 86740989—
SolventDichloromethaneHCID 6344—
Product2-[beta-(2-furyl)acrylamido]-N5-methyl-N1,N1-di(n-propyl)pentane-1,5-diamideHCID 8674099080%

Reaction Steps

In 75 ml of methylene chloride was dissolved 1.5 g of β-(2-furyl)acrylic acid, and 2.7 g of triethylamine and 1.3 g of ethyl chlorocarbonate were successively added thereto dropwise at -25° C. to -20° C. After 30 minutes, 3 g of the DL-2-amino-N5 -methyl-N1,N1 -di(n-propyl)-pentane-1,5-diamide hydrochloride was added to the above solution, and the resulting mixture was subjected to reaction at the same temperature for 30 minutes and at room temperature for 30 minutes. After completion of the reaction, the reaction mixture was washed successively with 30 ml of a 5% aqueous sodium hydroxide solution, 30 ml of diluted hydrochloric acid and 30 ml of water and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure to obtain 3.1 g (yield 80%) of DL-2-[β-(2-furyl)acrylamido]-N5 -methyl-N1,N1 -di(n-propyl)pentane-1,5-diamide having a melting point of 112°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04610983
Source datasetuspto-grants-1986_09
ORD IDord-47a1a8fa8c3e452ea1b4ee37c4296f87
Source noteuspto-grants-1986_09