HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetamide → HCID 13632727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 14911578 | HCID 14911578 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13632727 | HCID 13632727 | — |
Reaction Steps
To the total amount of the crude 2-acetyl-4methylcyclohexanone prepared in (1), 35 ml of ethanol, 3.36 g of cyanoacetamide and a small amount of piperidine were added and the obtained reaction mixture was heated under reflux for four hours. The crystals thus precipitated were filtered and recrystallized from a mixture of methanol and water to give 4.22 g of 4-cyano-1,7-dimethyl-2,3,5,6,7,8hexahydro-3-oxoisoquinoline. m.p. >290° C. NMRδTMSCF3COOH : 1.23 (3H, d), 2.60 (3H, s) and 1.8-3.3 (7H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824952 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-66ec3a147add45cbb1ebdd4deca14986 |
| Source note | uspto-grants-1989_04 |