HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12760922, compound → HCID 15729797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12760922 | HCID 12760922 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15729797 | HCID 15729797 | 86% |
Reaction Steps
A 100 ml autoclave was charged with 6.0 g of 7-hydroxy-2,4,4-trimethyl-4H-1-benzopyran synthesized by the method of Japanese Laid-Open Patent Publication No. 5475/1981, 1.0 g of 5% palladium-carbon and 20 ml of ethanol, and hydrogenation was carried out at 85° C. The resulting product was recrystallized from n-hexanetoluene to give 5.2 g (86%) of the desired product as colorless crystals (melting point 97°-98° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04838924 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-e6c2435877674706ba3cd34d5a9826bf |
| Source note | uspto-grants-1989_06 |