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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067793Generated: November 1, 2026

4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acid → Methyl 4-((((1,1-dimethylethoxy)carbonyl)amino)methyl)benzoate

https://huagongshe.com/reaction/1067793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
ProductMethyl 4-((((1,1-dimethylethoxy)carbonyl)amino)methyl)benzoateHCID 1422181783.6%

Reaction Steps

A mixture of 16.2 g (64.5 mmol) of 4-(tert-butoxycarbonylaminomethyl)benzoic acid, 13.6 g (70.9 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 1.00 g of 4-dimethylaminopyridine and 200 ml of methanol was stirred at room temperature for 4 hours. Methanol was distilled off under reduced pressure and ice water was poured to the residue thus obtained. The mixture was extracted twice with ethyl acetate and the extract was washed with 10% citric acid aqueous solution and then with saturated sodium hydrogencarbonate aqueous solution and finally with saturated sodium chloride aqueous solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 14.3 g (83.6%) of methyl 4-(tert-butoxycarbonylaminomethyl)-benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248772B1
Source datasetuspto-grants-2001_06
ORD IDord-cc6c83845fac4f26bc4784a5b6100436
Source noteuspto-grants-2001_06