HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-Benzamido-1-(2-benzoyloxyethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Hydroxyethyl)-4-benzamidopiperidine | HCID 20315176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Benzamido-1-(2-benzoyloxyethyl)piperidine | HCID 20315175 | 75% |
Reaction Steps
1.4 Milliliters (0.012 mol) of benzoylchloride were added to a stirred solution of 2.48 grams (0.01 mol) of 4-benzamido-1-(2-hydroxyethyl)piperidine and 2.8 milliliters (0.02 mol) of triethylamine in 10 milliliters of dichloromethane. The solution was stirred at room temperature for 2 hours, then washed with water, dried and evaporated. The residue was crystallised from n-butyl acetate to give 2.5 grams (75% yield) of the title compound m.p. 139°-40° C. Treatment of a solution of the base in ethanol with ethanolic hydrogen chloride precipitated the hydrochloride, m.p. 217°-18° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105666 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-56f7d3a66bf24851ad457838c707d613 |
| Source note | uspto-grants-1978_08 |