Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-(Methylsulfonyl)aniline hydrochloride | HCID 2735180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67132096 | HCID 67132096 | 22% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126941B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b6234051766a4ddd8d1f639bc823fb2e |
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| Source note | uspto-grants-2015_09 |
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