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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233702Generated: October 30, 2026

Cyclobutanone → HCID 67132096, compound

https://huagongshe.com/reaction/2233702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantSodium SulfateHCID 24436—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-(Methylsulfonyl)aniline hydrochlorideHCID 2735180—
SolventDimethylformamideHCID 6228—
ProductHCID 67132096HCID 6713209622%

Reaction Conditions

Temperature120 °C

Reaction Steps

Trimethylsilyl cyanide (0.4 g, 4 mmol) was added dropwise to a mixture of 4-methanesulfonylphenylamine hydrochloride (0.415 g, 2 mmol), cyclobutanone (0.28 g, 4-mmol) and sodium sulfate (1 g) in DMF (3 ml). The mixture was stirred for 15 hours at 120° C. After filtration to remove the sodium sulfate, the filtrate was washed with brine and extracted with ethyl acetate. The organic layer was concentrated and chromatographed (dichloromethane:acetone, 90:10) to yield 1-(4-methanesulfonylphenylamino)cyclobutanecarbonitrile (45a) (0.116 g, 0.44 mmol, 22%) as a yellowish solid. 4-methanesulfonylphenylamine (0.201 g, 1.17 mmol, 59%) was also recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709517B2
Source datasetuspto-grants-2010_05
ORD IDord-837abec53abd4556af500900af59e823
Source noteuspto-grants-2010_05