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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305230Generated: October 25, 2026

Methanol → Methyl 4-[2-(tert-butoxycarbonylamino)ethyl]benzoate

https://huagongshe.com/reaction/2305230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactanttrifluoro-methanesulfonic Acid 4-(2-tert-butoxycarbonylamino-ethyl)-phenyl EsterHCID 18459135—
Catalystpalladium(II) acetateHCID 167845—
ProductMethyl 4-[2-(tert-butoxycarbonylamino)ethyl]benzoateHCID 2271001376%

Reaction Conditions

Temperature78 °C

Reaction Steps

A mixture of 4-[2-(tert-butoxycarbonylamino)ethyl]-phenyl trifluoromethanesulfonate (6.11 g, 16.6 mmol), palladium(II) acetate (745 mg, 3.32 mmol), 1,3-bis-(diphenylphosphino)propane (1.37 g, 3.32 mmol), triethylamine (6.94 ml, 49.8 mmol), and MeOH (24ml) in DMF (60 ml) was purged for 30 min with carbon monoxide. The mixture was stirred under carbon monoxide atmosphere at 78° C. for 3 hours. After cooling the mixture to room temperature, the reaction mixture was diluted with EtOAc, washed with water, 1N-hydrochloric acid, water, saturated sodium hydrogencarbonate, water and brine successively, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane:EtOAc, 4:1-3:1) to give methyl 4-[2-(tert-butoxycarbonylamino)ethyl]benzoate (3.52 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437146B1
Source datasetuspto-grants-2002_08
ORD IDord-c9eea0ea7072494e89b772851a645535
Source noteuspto-grants-2002_08