HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromopyridine → HCID 21243518, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromopyridine | HCID 14268 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21243518 | HCID 21243518 | 82.6% |
Reaction Steps
35 ml of ether was cooled to -78° C. and 20 ml of a 1.6 M solution of n-butyllithium in hexane was added thereto. To the obtained mixture, 5 g of 4-bromopyridine dissolved in 30 ml of ether was added. Then 5 g of 1,4-cyclohexanedione monoethylene acetal dissolved in 30 ml of tetrahydrofuran was further added thereto. After the completion of the reaction, the reaction mixture was poured into a saturated aqueous solution of ammonium chloride and purified by extracting with chloroform to give 5 g of 4-hydroxy-4-(4-pyridyl)cyclohexanone
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824952 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-2cf68b5674c54e7a959836b16b919515 |
| Source note | uspto-grants-1989_04 |