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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009928Generated: October 26, 2026

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

https://huagongshe.com/reaction/1009928

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 diisopropyl ether to give the title compound (0.228 g) as a colorless powder with contamination.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973163B2
Source datasetuspto-grants-2011_07
ORD IDord-4c46f82b77324daf8eec824c259c7b85
Source noteuspto-grants-2011_07