HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178472385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 17963321 | HCID 17963321 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178472385 | HCID 178472385 | — |
Reaction Steps
Ethyl 4-[4-(3,4-dichlorophenoxy)-1-piperidinyl]-cyclohexanecarboxylate (method F, step a, 0.97 g) was added to a solution of sodium ethoxide prepared from sodium (1.28 g) and ethanol (100 ml). The resultant solution was heated under reflux for 18 h. Acetic acid (0.1 ml) was added and the solvent was evaporated. Ethyl acetate, water and sodium hydroxide were added to the residue and separated. The aqueous phase was extracted twice with ethyl acetate-methanol mixtures and the combined organic phases were washed with brine, dried (MgSO4), filtered and evaporated to give the subtitle compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307090B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-39345354f4a34b29ba087d8529347aa5 |
| Source note | uspto-grants-2007_12 |