HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Acetamide, N-(4-((1-methyl-4-phenyl-4-piperidinyl)oxy)phenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl- | HCID 3060392 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Acetamide, N-(4-((1-methyl-4-phenyl-4-piperidinyl)oxy)phenyl)- | HCID 3060397 | — |
Reaction Steps
A solution of 0.85 g of acetyl chloride in 5 ml of benzene is added dropwise to a solution of 2.8 g of 4-(4-aminophenoxy)-1-methyl-4-phenylpiperidine and 1.1 g of triethylamine in 10 ml of benzene. After stirring the mixture at room temperature for 6 hours, it is concentrated; the resulting residue is taken up with 30 ml each of water and diethyl ether; the obtained mixture is shaken thoroughly, and the organic phase is separated off, dried over sodium sulfate and concentrated. 2.8 g of the title compound remain as a viscous yellow oil which crystallizes (m.p. 143° to 144° C.) from diethylether after standing for several days.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04333942 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-870e1b1a003c4c58bf0b300d6fd1bbc5 |
| Source note | uspto-grants-1982_06 |