HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 23456202, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 23456179 | HCID 23456179 | — |
| Reactant | HCID 23456207 | HCID 23456207 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23456202 | HCID 23456202 | — |
Reaction Steps
Reduction of the latter with hydrogen over a palladium-on-charcoal catalyst; alkaline saponification of the resulting 3-(1,2,5-trimethyl-3-pyrrole)propionitrile; cyclization of the resulting 3-(1,2,5-trimethyl-3-pyrrole)propionic acid with polyphosphoric acid; reaction of the resulting 4-oxo-1,2,3-trimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrrole with methyl magnesium bromide; and reaction of the resulting 4-hydroxy-1,2,3,4-tetramethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrrole with potassium cyanide and potassium acetate in glacial acetic acid using the procedure described above in Example 10 affords 1,2,3,4-tetramethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrrole-4-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04239687 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-81c97de12a774da4b0f4dc117bcd40c4 |
| Source note | uspto-grants-1980_12 |