HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 21430573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 3,3-Diethoxypropyne | HCID 66285 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21430573 | HCID 21430573 | — |
Reaction Steps
4-Benzamidopiperidine (62 g.) was added to a stirred suspensions of 1.1 g. cupric acetate and 9.5 g. paraformaldehyde in 300 ml. dry dioxane, followed by propiolaldehyde diethylacetal (38.6 g.). Stirring was continued for 24 hours at 80° C. under nitrogen. The hot reaction mixture was filtered and the filtrate was evaporated. Recrystallisation of the solid residue from ethyl acetate-petroleum ether (bp. 60°-80° C.) gave 4-benzamido-1-(4,4-diethoxybut-2-ynyl)piperidine as colourless shining leaflets. (84.6 g.), m.p. 130° C. (Found: C, 69.5; H, 8.3; N, 8.3 C20H28N2O3 requires C, 69.7; H, 8.2; N, 8.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028365 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-b544f08b4c9a4cab9e8ffb2d875aa714 |
| Source note | uspto-grants-1977_06 |