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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644121Generated: October 27, 2026

4-Chloro-2-methylphenyl isocyanate → N-(4-chloro-2-methylphenyl)isoindoline-2-carboxamide

https://huagongshe.com/reaction/1644121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methylphenyl isocyanateHCID 142157—
ReactantIsoindolineHCID 422478—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-chloro-2-methylphenyl)isoindoline-2-carboxamideHCID 5752788494.2%

Reaction Steps

To a solution of isoindoline (238 mg, 2.0 mmol) in dry 1,4-dioxane (10 mL) was added 4-chloro-2-methylphenyl isocyanate (335 mg, 2.0 mmol) under argon at room temperature. The reaction mixture was then stirred at RT overnight. The solvent was evaporated under reduced pressure, and the residue was purified by recrystallization from ethanol to give the title compound (540 mg, 94%) as a white solid. 1H NMR (500 MHz, DMSO-d6): δ 2.24 (s, 2H), 4.76 (s, 4H), 7.20 (dd, J=2.5, 8.5 Hz, 1H), 7.27 (d, J=2.5 Hz, 1H), 7.30-7.32 (m, 2H), 7.34-7.37 (m, 2H), 7.42 (d, J=8.5 Hz, 1H), 7.84 (s, 1H); 13C NMR (DMSO-d6): δ 17.7, 51.9, 122.8, 125.6, 126.8, 127.3, 128.1, 129.5, 134.7, 136.8, 154.2; MS (MH+, 287); EA calc'd for C16H15ClN2O: C, 67.02; H, 5.27; N, 9.77. Found C, 66.82; H, 5.41; N, 9.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124121B2
Source datasetuspto-grants-2012_02
ORD IDord-083ec49ed21a4f439b43738b1096d27e
Source noteuspto-grants-2012_02