HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 1-Acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Acetyl-4-(4-fluorobenzoyl)piperidine | HCID 117257 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine | HCID 19100916 | 56.8% |
Reaction Steps
A mixture of 74.7 parts of 1-acetyl-4-(4-fluorobenzoyl)piperidine, 46.5 parts of 1,2-ethanediol, 3 parts of 4-methylbenzenesulfonic acid and 810 parts of benzene was stirred for 108 hours at reflux temperature using a water separator. After cooling, the reaction mixture was washed successively with 250 parts of water, 22.5 parts of ammonium hydroxide and 250 parts of water. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CHCl3 /CH3COCH3 50:50). The eluent of the desired fraction was evaporated, yielding 50 parts (56.8%) of 1-acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine (interm. 45).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05284854 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-2ea73cc2d0e74d2aaeb0c5b1c866b63f |
| Source note | uspto-grants-1994_02 |