HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-One | HCID 2735451 | — |
| Reactant | Methyl 4-amino-4-thioxobutanoate | HCID 18333020 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionate | HCID 18333015 | — |
Reaction Steps
2-(Bromoacetyl)benzofuran (650 ml) was added to an ethanol (12 ml) solution of methyl 4-amino-4-thioxobutyrate (400 mg), which was heated under reflux overnight. After cooling, water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was dried, concentrated, and then purified by silica gel column chromatography (eluent: hexane/ethyl acetate=4/1). The obtained crystals were washed with hexane to obtain ethyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionate (460 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329389B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-81ba8f4e2d634cbfbf9dcde51199b65d |
| Source note | uspto-grants-2001_12 |