HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 71278572, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | 6-Hydroxy-3-coumaranone | HCID 235717 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 71278572 | HCID 71278572 | 48.1% |
Reaction Steps
A solution of 6-hydroxybenzofuran-3(2H)-one (0.750 g, 5.00 mmol) in ethanol (5 mL) was added with 2-oxopiperazine (0.500 g, 5.00 mmol), and 37% aqueous formaldehyde (0.406 g, 5.00 mmol) at room temperature. The mixture was stirred overnight at room temperature, and then added with 37% aqueous formaldehyde (0.406 g, 5.00 mmol) at room temperature, and the mixture was refluxed for 4 hours by heating. The reaction mixture was cooled to room temperature, and then subjected to suction filtration to obtain 4-[(6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazin-2-one (0.631 g, 48%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-651a6c5200884ee1be1157c47f4a5b24 |
| Source note | uspto-grants-2015_10 |