HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 13019528, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13019513 | HCID 13019513 | — |
| Reactant | HCID 70544040 | HCID 70544040 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13019528 | HCID 13019528 | — |
Reaction Steps
A mixture of 23.6 g. (0.06 mol) methyl 2-[3-(4-benzamidopiperidino)-propoxy]-benzoate (see Example 2a), 200 ml. ethanol and 200 ml. 1 N aqueous sodium hydroxide solution is heated under reflux for 1 hour, then evaporated and the evaporation residue dissolved in water and acidified with dilute hydrochloric acid. This is followed by extraction with a mixture of 9 parts by volume of methylene chloride and 1 part by volume of ethanol. The extract is evaporated and the residue obtained is taken up in acetone and the hydrochloride of the desired product is precipitated out by the addition of ethereal hydrochloric acid. There are obtained 14.5 g. (59% of theory) 2-[3-(4-benzamidopiperidino)-propoxy]-benzoic acid hydrochloride; m.p. 207°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04348401 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-7fa5a7291a474822b144ab8997f23967 |
| Source note | uspto-grants-1982_09 |