Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919297Generated: November 4, 2026

Triethylamine → 4-(4,4-Dimethyl-5-imino-2-oxo-1-imidazolidinyl)-2-trifluoromethyl-benzonitrile

https://huagongshe.com/reaction/1919297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-methylpropionitrileHCID 88022—
Reactant4-Isocyanato-2-(trifluoromethyl)benzonitrileHCID 11063739—
Solvent1,2-DichloroethaneHCID 11—
Product4-(4,4-Dimethyl-5-imino-2-oxo-1-imidazolidinyl)-2-trifluoromethyl-benzonitrileHCID 2211694847.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of compound 9 (641 mg, 7.62 mmol) and triethylamine (168 mg, 1.66 mmol) in 1,2 dichloroethane (8.4 mL) at 0° C. under argon was dropwise added a solution of the isocyanate 8a (1.54 g, 7.28 mmol) in 1,2 dichloroethane (3.5 mL). The solution was stirred at 0° C. for 35 min and the ice bath was then removed and stirred at room temperature for an additional 30 min. The solution was then evaporated to dryness and purified by flash chromatography using EtOAc/Hexane (6:4) as an eluant to give pure compound 10a (1.02 g, 47%). 1H NMR (300 MHz, Acetone-d6) δ: 1.54 (m, 6H), 7.45 (broad s, 1H), 8.12 (d, 1H, J=8.46 Hz), 8.29 (dd, 1H, J1=6.90 Hz, J2=1.61 Hz), 8.46 (s, 1H), 8.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168627B2
Source datasetuspto-grants-2012_05
ORD IDord-2ea9b9cc3a25451b94dd4117a7368cd1
Source noteuspto-grants-2012_05