HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Cyclohexanedione → HCID 11644071, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11644071 | HCID 11644071 | 56.5% |
Reaction Steps
202 mg of 4-hydroxypiperidine and 448 mg of 1,4-cyclohexanedione were heated under reflux in 10 ml of ethanol and reacted for 9 hours with introducing air with a pump. During the reaction, ethanol was added as needed. After the completion of the reaction, the resultant was separated by silica gel column chromatography (n-hexane:ethyl acetate=2:1) and 0.218 g of 1-(4-hydroxyphenyl)-4-hydroxypiperidine was obtained (yield 56.48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750156B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-5ef6a960cace4d96a695667a3d43808c |
| Source note | uspto-grants-2010_07 |