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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735753Generated: October 25, 2026

Phenyl isocyanate → {1-[(Anilinocarbonyl)amino]cyclohexyl}acetic acid

https://huagongshe.com/reaction/735753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantSodium HydroxideHCID 14798—
Reactant2-(1-Aminocyclohexyl)acetic acid hydrochlorideHCID 4426693—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product{1-[(Anilinocarbonyl)amino]cyclohexyl}acetic acidHCID 5784712055.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of (1-aminocyclohexyl)acetic acid (0.232 mg, 1.48 mmol) in a mixture of 1,4-dioxane (9 ml) and water (3 ml) was added 30% aqueous sodium hydroxide solution to pH 9. Phenylisocyanate (0.24 ml, 2.22 mmol) was added dropwise at 35° C. and 30% aqueous sodium hydroxide solution was added to adjust the solution to pH9. The reaction mixture was stirred at 40° C. for 1.5 hrs and concentrated under reduced pressure. 5N Hydrochloric acid was added to acidify the solution (pH3) and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried (over anhydrous MgSO4). After concentration under reduced pressure, the precipitated solid was collected by filtration and washed with diisopropy ether to give the title compound (0.228 g) as a colorless powder with contamination.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592453B2
Source datasetuspto-grants-2009_09
ORD IDord-18a11ff324034116812272839d18149a
Source noteuspto-grants-2009_09