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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711679Generated: October 30, 2026

Benzoyl isocyanate → N-(2-cyanocyclopent-1-enylcarbamoyl)benzamide

https://huagongshe.com/reaction/711679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isocyanateHCID 78210—
Reactant2-Amino-1-cyclopentene-1-carbonitrileHCID 287275—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-cyanocyclopent-1-enylcarbamoyl)benzamideHCID 5745693776.2%

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) δ 11.33 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-81bbc677e7d7424bad72576f3dd3ea55
Source noteuspto-grants-2015_11