HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466146Generated: November 2, 2026
5-(2-Bromoethyl)-2-benzofuran-1(3H)-one → 1,4-Bis[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one
https://huagongshe.com/reaction/1466146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one | HCID 67513163 | — |
| Reactant | 1-[2-(1,3-Dihydro-1-oxo-5-isobenzofuranyl)ethyl]-2-piperazinone | HCID 117599333 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,4-Bis[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one | HCID 89533479 | — |
Reaction Steps
To a solution of 1-[2-(1-Oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-2-one (30 mg, 0.12 mmol) and 5-(2-Bromoethyl)-2-benzofuran-1(3H)-one (56 mg, 0.23 mmol) in DMF (2 ml) was added TEA (0.048 ml, 0.35 mmol) and tetrabutylammonium iodide (4.3 mg, 0.012 mmol). The mixture was heated to 55° C. for 16 hours. LC showed formation of the desired product, which was purified by mass-directed reverse phase HPLC (AcCN-Water with 0.1% TFA). LC-MS (IE, m/z): 421 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999990B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-21c76461506a46b0a0487a8f880d9d7e |
|---|
| Source note | uspto-grants-2015_04 |
|---|