HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412295Generated: October 30, 2026
Ammonium formate → {2-[3-((R)-2-Aminopropyl)phenyl]ethyl}carbamic Acid tert-Butyl Ester
https://huagongshe.com/reaction/2412295
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | (2-{3-[(R)-2-((R)-1-phenylethylamino)propyl]phenyl}ethyl)carbamic acid tert-butyl ester | HCID 66781838 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {2-[3-((R)-2-Aminopropyl)phenyl]ethyl}carbamic Acid tert-Butyl Ester | HCID 66782120 | — |
Reaction Steps
A stirred solution of (2-{3-[(R)-2-((R)-1-phenylethylamino)propyl]phenyl}ethyl)-carbamic acid tert-butyl ester (1.54 g, 4.02 mmol), palladium hydroxide on carbon (10 wt. %, ˜50% water, 2.24 g, 0.805 mmol), and ammonium formate (1.27 g, 20.1 mmol) in EtOH (50.0 mL) was heated gradually to 50° C. and then stirred at 50° C. for 1.5 h. The reaction mixture was filtered through a pad of Celite and the filtrate was concentrated under reduced pressure to give the title compound, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816088B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-88dba7251d9046f985d5851d647b43fa |
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| Source note | uspto-grants-2014_08 |
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