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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680396Generated: October 30, 2026

Potassium Cyanide → HCID 23456202, compound

https://huagongshe.com/reaction/1680396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 23456179HCID 23456179—
ReactantHCID 23456207HCID 23456207—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178418573HCID 178418573—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 23456202HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273713
Source datasetuspto-grants-1981_06
ORD IDord-8cf139fc483146cfa23dde94386ae1c6
Source noteuspto-grants-1981_06