HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → 3(2H)-Benzofuranone, 6-hydroxy-2-[(3-hydroxyphenyl)methylene]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Hydroxy-3-coumaranone | HCID 235717 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3(2H)-Benzofuranone, 6-hydroxy-2-[(3-hydroxyphenyl)methylene]- | HCID 490059 | 70.9% |
Reaction Steps
After 6-hydroxy-2H-benzofuran-3-one 1 g and 3-hydroxybenzaldehyde 0.813 g were dissolved in methanol 75 ml, concentrated hydrochloric acid 50 ml was added, and the mixture was refluxed for two hours. The solution was cooled to room temperature, water 400 ml was added and allowed to stand for one hour. Precipitated crystals were filtered. The crystals were dried over phosphorous pentoxide at a temperature of 60° C. for five hours under reduced pressure to obtain the desired compound 1.20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06143779 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-1fd35ca8fae141c3a5cac3f5fd0cbf6d |
| Source note | uspto-grants-2000_11 |