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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | trifluoro-methanesulfonic Acid 4-(2-tert-butoxycarbonylamino-ethyl)-phenyl Ester | HCID 18459135 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | Methyl 4-[2-(tert-butoxycarbonylamino)ethyl]benzoate | HCID 22710013 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06437146B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-c9eea0ea7072494e89b772851a645535 |
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| Source note | uspto-grants-2002_08 |
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