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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732849Generated: October 29, 2026

Potassium Cyanide → HCID 23456202, compound

https://huagongshe.com/reaction/1732849

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 numberUS04239687
Source datasetuspto-grants-1980_12
ORD IDord-81c97de12a774da4b0f4dc117bcd40c4
Source noteuspto-grants-1980_12