HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Carbonyldiimidazole → 2-(t-Butylamino)ethyl 2-phenylbenzofuran-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-(tert-Butylamino)ethanol | HCID 78361 | — |
| Reactant | 2-Phenylbenzofuran-7-carboxylic acid | HCID 14229706 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(t-Butylamino)ethyl 2-phenylbenzofuran-7-carboxylate | HCID 14229807 | 84.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829067 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-1e2808da575d4693abce88953851768c |
| Source note | uspto-grants-1989_05 |