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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515921Generated: October 27, 2026

4-(2-Aminoethyl)benzoic acid → 4-(2-{[(Tert-butoxy)carbonyl]amino}ethyl)benzoic acid

https://huagongshe.com/reaction/515921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Aminoethyl)benzoic acidHCID 506066—
ReactantTert-butyldicarbonateHCID 22064466—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-{[(Tert-butoxy)carbonyl]amino}ethyl)benzoic acidHCID 16640905—

Reaction Steps

tert-Butyl dicarbonate (1.64 g; 7.5 mmol) is dissolved in 1,4-dioxane (5 mL) and the solution is added to a well-stirred solution of 4-(2-aminoethyl)benzoic acid (1.0 g; 5 mmol) in 1M aqueous sodium hydroxide solution (25 mL) and 1,4-dioxane (10 mL), and the mixture is then stirred at ambient temperature for 3 hours. The 1,4-dioxane is removed by evaporation in vacuo, and then ethyl acetate (200 mL) is added to the residue. The pH of the aqueous phase is adjusted to 1.5 with 2M aqueous HCl solution. The organic phase is separated off and the aqueous phase is then extracted with ethyl acetate (100 mL). The combined organic extracts are washed with water, dried over Na2SO4 and evaporated to a volume of 10 mL. Heptane is added to the residue and then the solid precipitate is filtered off to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-936255d934364548afffe4f4747b54e7
Source noteuspto-grants-2015_08