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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077901Generated: October 30, 2026

Triethylamine → N-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline

https://huagongshe.com/reaction/1077901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
ReactantN-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)anilineHCID 19065098—
SolventDichloromethaneHCID 6344—
ProductN-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)anilineHCID 86749721—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To the mixture of the obtained N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline (3.2 g), triethylamine (1.2 ml) and dichloromethane (60 ml), was added dropwise a solution of ethyl chloroglyoxylate (0.9 ml) in dichloromethane (10 ml) at -65° C. The reaction solution was stirred for 1 hour at -40° C., and then ice-water (50 ml) was added thereto to fractionate. The dichloromethane layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to give N-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline (3.1 g) as colorless powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545652
Source datasetuspto-grants-1996_08
ORD IDord-b95d4634d2204752abf51f73a4d1fd28
Source noteuspto-grants-1996_08