HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 2-(Diisopropylamino)ethyl 2-phenylbenzofuran-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloroethyldiisopropylammonium chloride | HCID 77942 | — |
| Reactant | 2-Phenylbenzofuran-7-carboxylic acid | HCID 14229706 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Diisopropylamino)ethyl 2-phenylbenzofuran-7-carboxylate | HCID 14229767 | 84.9% |
Reaction Steps
A mixture of 1.16 g of 2-phenylbenzofuran-7-carboxylic acid, 1.0 g of 2-(diisopropylamino)ethyl chloride hydrochloride, 0.66 g of potassium hydroxide and 20 ml of isopropanol is refluxed for 1 hour. After cooling, ethyl acetate and water are added to the reaction mixture. The organic layer is collected, washed with a saturated sodium chloride solution and evaporated to remove solvent. The residue is purified by silica gel column chromatography (solvent; chloroform:methanol=20:1) to give 1.51 g 2-(diisopropylamino)ethyl 2-phenylbenzofuran-7-carboxylate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829067 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-3db9825a54ae4ac6bd36322a9eaf447b |
| Source note | uspto-grants-1989_05 |