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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504962Generated: November 2, 2026

Cyclobutanone → 4-(4-((2-Cyanopropan-2-yl)amino)-2-fluorophenyl)butanenitrile

https://huagongshe.com/reaction/1504962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-(4-Amino-2-fluorophenyl)butanenitrileHCID 57672609—
CatalystZincchlorideHCID 3007855—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-((2-Cyanopropan-2-yl)amino)-2-fluorophenyl)butanenitrileHCID 6873421295.9%

Reaction Steps

TMSCN (0.14 mL, 1.01 mmol) was added to a mixture of the compound 68 (60 mg, 0.34 mmol), cyclobutanone (0.15 mL, 2.04 mmol) and ZnCl2 (4 mg, 0.04 mmol) in dioxane (1 mL) with stirring. The reaction mixture was stirred at room temperature for 1 h, and concentrated in vacuo. The residue was diluted with water, and extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to dryness to give compound 70 (80 mg, 91%) as a light yellow oil. The crude product was used directly for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216957B2
Source datasetuspto-grants-2015_12
ORD IDord-98eae07e7c6242a58aa77f98394f20dc
Source noteuspto-grants-2015_12