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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968444Generated: October 30, 2026

4-Aminobenzoic Acid → 4-[(Cyclohexylcarbonyl)amino]benzoic acid

https://huagongshe.com/reaction/1968444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 4400321HCID 4400321—
SolventTetrahydrofuranHCID 8028—
Product4-[(Cyclohexylcarbonyl)amino]benzoic acidHCID 74573392%

Reaction Steps

A mixture of 4-aminobenzoic acid 48a (1.98 mmol, 300 mg), cyclohexanecarbonyl chloride 48b (1.98 mmol, 291 mg), and Et3N (2.52 mmol, 0.43 mL) in 6 mL of THF was stirred at room temperature overnight. 1N aqueous NaOH (7.9 mmol, 7.9 mL) was added to the mixture (containing methyl 4-(cyclohexanecarboxamido)benzoate 48c) and the reaction mixture was stirred for 5 h at room temperature. The THF was removed by rotary evaporation and 1N aqueous HCl was added to precipitate the product, which was filtered to give 480 mg (92%) of 48d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426401B2
Source datasetuspto-grants-2013_04
ORD IDord-cc78b025a5664bf49287d922fb1b73fa
Source noteuspto-grants-2013_04