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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795171Generated: November 4, 2026

Sodium Cyanide → HCID 21023772, compound

https://huagongshe.com/reaction/1795171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantHCID 21023777HCID 21023777—
SolventEthanolHCID 702—
ProductHCID 21023772HCID 2102377242%

Reaction Steps

A solution of 4-cyclohexyl-4-(3-oxo-propyl)-piperidine-1-carboxylic acid tert-butyl ester, 10, (300 mg, 0.93) in ethanol (10 ml) is treated with tosylmethyl isocyanide (tosMIC) (176 mg, 0.93 mmole) and sodium cyanide (6 mg) at room temperature for three hours. The solvent is removed under reduced pressure and ammonia in methanol (2M, 10 ml) added. The mixture is stirred in a sealed tube overnight. The reaction mixture is then concentrated under reduced pressure and the residue taken up in chloroform, washed with aqueous sodium bicarbonate, brine, then dried with sodium sulfate and concentrated to a red oil. The residue is purified over silica (methylene chloride:methanol=15:1, Rf=0.58) to afford 141 mg (42% yield) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026335B2
Source datasetuspto-grants-2006_04
ORD IDord-ccdd26bae6114da5aa40a2155169759f
Source noteuspto-grants-2006_04