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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570613Generated: October 28, 2026

Citric Acid → HCID 66732569, compound

https://huagongshe.com/reaction/570613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantAminoisobutyric acidHCID 6119—
ReactantPotassium CarbonateHCID 11430—
Reactant2-AcetylcyclohexanoneHCID 13400—
ReactantHCID 24708843HCID 24708843—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66732569HCID 6673256994.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

The title compound, made in accordance with General Method 3, may be used to prepare compound 4 in accordance with General Method 1. 4-Bromo-N-butyl-2-fluorobenzamide (950 mg, 3.22 mmol), 2-aminoisobutyric acid (450 mg, 4.36 mmol), CuI (100 mg, 0.5 mmol), TEA (0.1 mL) and K2CO3 (1.0 g, 7.2 mmol) were charged in DMF (8 mL) and water (2 mL) and stirred at RT for 5 min. 2-Acetylcyclohexanone (100 mg, 0.7 mmol) was added and the reaction mixture was heated at 100° C. for 18 h. The reaction mixture was acidified with 1 M citric acid (pH 4) and extracted with ethyl acetate (50 mL, 2 times). The combined organic layer was dried over Na2SO4 and concentrated to obtain 900 mg of 2-(4-(butylcarbamoyl)-3-fluorophenylamino)-2-methylpropanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023869B2
Source datasetuspto-grants-2015_05
ORD IDord-bc2a4e409e4245499351f7afd5a90664
Source noteuspto-grants-2015_05