HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl isocyanate → N-(2-cyanocyclopent-1-enylcarbamoyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl isocyanate | HCID 78210 | — |
| Reactant | 2-Aminocyclopent-1-ene-1-carbonitrile | HCID 287275 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(2-cyanocyclopent-1-enylcarbamoyl)benzamide | HCID 57456937 | 76.2% |
Reaction Steps
To a solution of 2-aminocyclopent-1-enecarbonitrile (400 mg, 3.7 mmol) in 1.4-dioxane (20 mL) was added benzoyl isocyanate (545 g, 3.7 mmol). The reaction mixture was then stirred at room temperature under nitrogen overnight. The precipitate was collected by filtration, washed with 1.4-dioxane, and dried to give N-(2-cyanocyclopent-1-enylcarbamoyl)benzamide (720 mg, 76%) as a white solid. 1H NMR (400 MHz, CDCl3) δ11.33 (s, 1H), 11.22 (brs, 1H), 7.99-7.97 (m, 2H), 7.67-7.63 (m, 1H), 7.54-7.51 (m, 2H), 3.04-3.0 (m, 2H), 2.51-2.47 (m, 2H) 1.95-1.90 (m, 2H). MS 256 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541421B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-006eac9d25614c4c8ac3ea2cdb6cfe22 |
| Source note | uspto-grants-2013_09 |