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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510160Generated: November 4, 2026

Cyclohexyl isocyanide → HCID 178455701, compound

https://huagongshe.com/reaction/1510160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanideHCID 79129—
Reactant3-Fluorophenylamine hydrochlorideHCID 2755765—
ReactantPotassium cyanateHCID 11378442—
ReactantHCID 66790112HCID 66790112—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178455701HCID 178455701—

Reaction Steps

1-(3-isopropoxybenzyl)-2-vinylpiperidin-4-one (7.00 g, 25.6 mmol) in methanol (14 ml) was added cyclohexyl isocyanide (3.17 ml, 25.6 mmol) then potassium cyanate (2.08 g, 25.6 mmol) in water (5 ml) was added. 3-Fluoroaniline hydrochloride (3.78 g, 25.6 mmol) was then added at 0° C. The mixture was stirred at rt for 12 hrs. The reaction was incomplete and another half equivalent of cyclohexyl isocyanide (1.59 ml, 12.8 mmol), potassium cyanate (1.04 g, 12.8 mmol), and 3-fluoroaniline hydrochloride (1.89 g, 12.8 mmol) was added. The mixture stirred for an additional twelve hours. The solution was concentrated and purified on silica gel 7% methanol/chloroform with 0.1% triethylamine. The impure product was purified a second time by flash chromatography on silica gel starting with 50% ethyl acetate/hexanes to 100% ethyl acetate. The diastereomers were resolved on a Chiral AD column 10% ethanol/hexanes with 0.3% diethylamine 250 ml/min at 250 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211904B2
Source datasetuspto-grants-2012_07
ORD IDord-d57fd99f377a42fe926833ef7ecc89ab
Source noteuspto-grants-2012_07