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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364754Generated: October 30, 2026

Cyclopentanone → methyl (2S)-2-(cyclopentylamino)butanoate

https://huagongshe.com/reaction/2364754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanoneHCID 8452—
ReactantSodium CarbonateHCID 10340—
ReactantSodium AcetateHCID 517045—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 2-aminobutanoate, (2S)-HCID 10820508—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productmethyl (2S)-2-(cyclopentylamino)butanoateHCID 6872858378.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-6bd5a054f0d94c0d8384024c4b19e71c
Source noteuspto-grants-2014_04