Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761915Generated: October 26, 2026

1,1'-Carbonyldiimidazole → 2-(t-Butylamino)ethyl 2-phenylbenzofuran-7-carboxylate

https://huagongshe.com/reaction/1761915

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(tert-Butylamino)ethanolHCID 78361—
Reactant2-Phenylbenzofuran-7-carboxylic acidHCID 14229706—
SolventTetrahydrofuranHCID 8028—
Product2-(t-Butylamino)ethyl 2-phenylbenzofuran-7-carboxylateHCID 1422980784.9%

Reaction Steps

1.43 g of 2-phenylbenzofuran-7-carboxylic acid are dissolved in 10 ml of tetrahydrofuran, and 1.08 g of carbonyldiimidazole are added to the solution. The mixture is stirred at room temperature for 2 hours and a solution of 0.76 g of 2-(t-butylamino)ethanol in 4 ml of tetrahydrofuran is added thereto. The mixture is stirred at room temperature for 15 hours and evaporated to remove solvent. Water is added to the residue and the aqueous mixture is extracted with ethyl acetate. The extract is washed with water, dried, and evaporated to remove solvent to give 1.72 g of 2-(t-butylamino)ethyl 2-phenylbenzofuran-7-carboxylate as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829067
Source datasetuspto-grants-1989_05
ORD IDord-1e2808da575d4693abce88953851768c
Source noteuspto-grants-1989_05