HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64456Generated: October 29, 2026
Ammonium formate → methyl 3-[(2S)-2-aminopropyl]benzoate
https://huagongshe.com/reaction/64456
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | methyl 3-[(2S)-2-{[(1S)-1-phenylethyl]amino}propyl]benzoate | HCID 86713469 | — |
| Catalyst | HCID 178420936 | HCID 178420936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | methyl 3-[(2S)-2-aminopropyl]benzoate | HCID 86713468 | 98.9% |
Reaction Steps
To a solution of 280 mg of methyl 3-[(2S)-2-{[(1S)-1-phenylethyl]amino}propyl]benzoate in 6.8 ml of ethanol were added 30 mg of 20% palladium-carbon hydroxide (wet) and 320 mg of ammonium formate, followed by stirring at 80° C. for 4 hours. The reaction mixture was filtered over Celite and the solvent was then evaporated under reduced pressure. To the obtained residue were added a saturated aqueous sodium hydrogen carbonate solution and chloroform to carry out a layer separation operation, followed by drying over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain 180 mg of methyl 3-[(2S)-2-aminopropyl]benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447090B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-6aa1473429484d83946237626c3c6865 |
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| Source note | uspto-grants-2016_09 |
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