HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865316Generated: October 26, 2026
Ammonium Acetate → methyl (3R)-3-amino-4-phenylbutanoate
https://huagongshe.com/reaction/1865316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Methyl 3-oxo-4-phenylbutanoate | HCID 2760261 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl (3R)-3-amino-4-phenylbutanoate | HCID 10081308 | — |
Reaction Steps
Ru(OAc)2((R)-dm-binap) (0.248 g, 0.260 mmol), methyl 3-oxo-4-phenylbutanoate (10.00 g, 52.0 mmol), ammonium acetate (4.01 g, 52.0 mmol) and methanol (50 mL) were placed in a 200 mL stainless steel autoclave under nitrogen atmosphere, and the mixture was stirred at 80° C. for 2 hours. The reaction mixture was cooled down to room temperature and further stirred under a hydrogen pressure of 3 MPa at 80° C. for 14 hours. After completion of the reaction, the solvent was removed by evaporation to give methyl (3R)-3-amino-4-phenylbutanoate as a crude material (13.01 g). The enantiomeric excess of methyl (3R)-3-amino-4-phenylbutanoate in the crude product was determined to be 94.7% ee by HPLC analysis using a SUMICHIRAL OA-4100R column after conversion into methyl (3R)-3-(4-nitrobenzoylamino)-4-phenylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626034B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-9e6686f33d584189b4ab82674c0cb643 |
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| Source note | uspto-grants-2009_12 |
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