HuagongsheHuagongshe Chemistry Print Report · For research reference only
2'-Hydroxyacetophenone → 3-Formylchromone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2'-Hydroxyacetophenone | HCID 8375 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Product | 3-Formylchromone | HCID 87112 | — |
Reaction Steps
In 80 volume parts of diemthylformamide there is dissolved 25 parts of orthohydroxyacetophenone and while the solution is externally cooled to about -20°C with dry ice-acetone, 80 volume parts of tetrachloropyrophosphate is added in small installments. The mixture is stirred at room temperature for 13 hours. The reaction mixture is then poured into ice-water and the resulting crystals are recovered by filtration, washed with water and ethanol and finally recrystallized from acetone. There is obtained a 19.6 parts yield of 4-oxo-4H-1-benzopyran-3-carboxaldehyde, as colorless crystals, melting at 152°-153°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03984441 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-f0a4136b7341424fa91412a1e15f60d6 |
| Source note | uspto-grants-1976_10 |