HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364754Generated: October 30, 2026
Cyclopentanone → methyl (2S)-2-(cyclopentylamino)butanoate
https://huagongshe.com/reaction/2364754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 2-aminobutanoate, (2S)- | HCID 10820508 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl (2S)-2-(cyclopentylamino)butanoate | HCID 68728583 | 78.4% |
Reaction Steps
Methyl (2S)-2-aminobutanoate 41b (18.74 g, 0.12 mol) was dissolved in 280 mL of dichloromethane. The reaction solution was cooled down to 0° C. in an ice-water bath followed by the addition of sodium acetate (5 g, 0.061 mol), cyclopentanone (10.78 g, 0.13 mol) and sodium triacetoxyborohydride (31 g, 0.16 mol) successively. The reaction solution was heated to room temperature and stirred for 4 hours. The reaction solution was poured into 150 mL of water, added dropwise with saturated sodium carbonate solution to adjust pH to 11 to 12 and seperated. The aqueous phase was extracted with dichloromethane (150 mL×2). The combined organic phase was washed with saturated brine (100 mL×2), then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure to obtain the title compound methyl (2S)-2-(cyclopentylamino)butanoate 4k (17.42 g, yield: 77.1%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691822B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-6bd5a054f0d94c0d8384024c4b19e71c |
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| Source note | uspto-grants-2014_04 |
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