HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 2-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-((4-Chlorophenyl)(4-piperidinyloxy)methyl)pyridine | HCID 11141197 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanol | HCID 15055855 | 56% |
Reaction Steps
1.00 g (3.30 mmol) of 4-[(4-chlorophenyl)-2-pyridylmethoxy]piperidine and 0.49 g (3.92 mmol) of 2-bromoethanol were dissolved in 10 ml of acetone, and 0.55 g (3.98 mmol) of potassium carbonate was added to the mixed solution. The mixture was stirred at room temperature for 15 hours. After the reaction, the insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was separated by silica gel column chromatography using a mixture of chloroform and methanol in the volume ratio 20:1 as the eluent. The desired fraction was concentrated under reduced pressure to give 0.64 g (56%) of 2-[4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929618 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-ad93b1a26b8c4b6c87d82aafe320b6cc |
| Source note | uspto-grants-1990_05 |