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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64927Generated: October 27, 2026

Triethylamine → 2-[beta-(2-furyl)acrylamido]-N1,N1,N5,N5-tetramethyl-pentane-1,5-diamide

https://huagongshe.com/reaction/64927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantEthyl chloroformateHCID 10928—
ReactantN-[beta-(2-furyl)acryloyl]glutamic acidHCID 54218369—
SolventDichloromethaneHCID 6344—
Product2-[beta-(2-furyl)acrylamido]-N1,N1,N5,N5-tetramethyl-pentane-1,5-diamideHCID 7318228655%

Reaction Steps

In 100 ml of methylene chloride was suspended 5 g of the DL-N-[β-(2-furyl)acryloyl]glutamic acid, and 7 g of triethylamine was added to dissolve it. Subsequently, the resulting solution was cooled to -20° C. to -15° C., after which 4.6 g of ethyl chlorocarbonate was added dropwise, and the resulting mixture was subjected to reaction for 30 minutes. Thereafter, 3.1 g of dimethylamine hydrochloride was added, and the resulting mixture was subjected to reaction at the same temperature for 2 hours. After completion of the reaction, the reaction mixture was washed successively with 50 ml of a 5% aqueous sodium hydroxide solution, 50 ml of diluted hydrochloric acid and 50 ml of water, and dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure to obtain 3.5 g (yield 55%) of DL-2-[β-(2-furyl)acrylamido]-N1,N1,N5,N5 -tetramethyl-pentane-1,5-diamide having a melting point of 178°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04610983
Source datasetuspto-grants-1986_09
ORD IDord-be6dec1f2e7545998c3db39245b54026
Source noteuspto-grants-1986_09