HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20386045, compound → 4-[4-Acetyl-7-(1-hydroxycyclohexyl)heptyl]benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20386045 | HCID 20386045 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[4-Acetyl-7-(1-hydroxycyclohexyl)heptyl]benzoic Acid | HCID 20386102 | — |
Reaction Steps
4-[4-Acetyl-7-(1-hydroxycyclohexyl)-6-heptyn-1-yl]benzoic acid (5.1 g., 0.014 mole) in ethyl acetate (55 ml.) is hydrogenated over 2.0 g. of a 5% Pt on charcoal catalyst at 1 atmosphere pressure and room temperature. The theoretical amount of hydrogen (0.028 mole) is absorbed in 25 minutes. The catalyst is filtered off, the solvent is evaporated and the residue (5 g.) is chromatographed on 75 g. of silica gel with 2% methanol in chloroform as eluant. The title compound is obtained as a colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04175203 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-9bef69d21ba64b87b32faa6c415676bd |
| Source note | uspto-grants-1979_11 |