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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(2-Aminoethyl)benzoic acid | HCID 506066 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(2-{[(Tert-butoxy)carbonyl]amino}ethyl)benzoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108983B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-936255d934364548afffe4f4747b54e7 |
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| Source note | uspto-grants-2015_08 |
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