HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ascofuranone → HCID 23134887, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ascofuranone | HCID 6434242 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23134887 | HCID 23134887 | — |
Reaction Steps
An ethanol (201 ml) solution of ascofuranone (1,058 mg, 2.52 mmlo) was stirred in the presence of 5% Pd/C (435 mg) in a hydrogen atmosphere at 0(C for three hours. After the catalyst was separated by filtration with the use of Celite, the filtrate was concentrated to obtain a crude product (1,178 mg). This product was purified by silica gel column chromatography (hexane:ethyl acetate═5:1) to obtain 3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-7-(tetrahydro-5,5-dimethyl-4-oxo-2-furanyl)-octyl]benzaldehyde (a diastereomeric mixture, yellow syrup 262 mg, yield 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07622598B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-5a6da47d821b44999f610e74ae848410 |
| Source note | uspto-grants-2009_11 |