HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 14985924, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4H-1-Benzopyran-6-carboxaldehyde, 7-hydroxy-5-methoxy-2-methyl-4-oxo- | HCID 81792 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14985924 | HCID 14985924 | 80% |
Reaction Steps
2.6 g (53 mmol) of sodium cyanide and then 18.50 g (223 mmol, 25 eq.) of activated manganese dioxide are added to 2 g (8.5 mmol) of 6-formyl-7-hydroxy-5-methoxy-2-methyl-4H -benzopyran-4-one (A. SCHONBERG, N. BADRAN and N. A. STARKONSKY, J. Am. Chem. Soc., 1953, 75, 4992) suspended in 105 ml of methanol acidified with 2.6 ml of acetic acid. After having been stirred for 4 hours at room temperature, the reaction mixture, diluted with 200 ml of ethyl acetate, is filtered to remove insoluble material (excess MnO2) and the solvents are evaporated. The powdery residue is taken up in water and filtered. 1.80 g of a beige powder are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05409952 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-21a3ecab3e8e4eb2b075bde5701355d3 |
| Source note | uspto-grants-1995_04 |