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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364763Generated: November 1, 2026

Acetone → methyl (2S)-2-(isopropylamino)butanoate

https://huagongshe.com/reaction/2364763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium CarbonateHCID 10340—
ReactantSodium AcetateHCID 517045—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantL-2-aminobutyrateHCID 6857370—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productmethyl (2S)-2-(isopropylamino)butanoateHCID 86668259159.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

(2S)-2-Aminobutanoate 41b (13.14 g, 85.52 mmol) was dissolved in 200 mL of dichloromethane. The reaction solution was cooled down to 0° C. in an ice-water bath followed by the addition of sodium acetate (3.51 g, 42.76 mmol), acetone (5.96 g, 0.10 mol) and sodium triacetoxyborohydride (21.75 g, 0.10 mol) successively. The reaction solution was heated to room temperature and stirred for 4 hours. The resulting solution was added with 100 mL of water, added dropwise with saturated sodium carbonate solution to adjust pH to 11 to 12 and separated. 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 methyl (2S)-2-(isopropylamino)butanoate 43a (10.85 g, yield: 79.7%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-d371c9a0182d40848fc4a91412742eb9
Source noteuspto-grants-2014_04