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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55762Generated: October 30, 2026

L-Leucine → N-Carbomethoxy-L-leucine

https://huagongshe.com/reaction/55762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-LeucineHCID 6106—
ReactantMethyl chloroformateHCID 6586—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ProductN-Carbomethoxy-L-leucineHCID 13821106—

Reaction Conditions

Temperature0 °C

Reaction Steps

An aqueous NaOH (1M, 2.6 mL) solution is added, while stirring, to L-Leucine (4 g, 30.5 mmol) in a round bottom flask (250 mL). To this solution was added sodium carbonate (1.62 g, 15.2 mmol). The flask is cooled to 0° C. in an ice-water bath. Methyl chloroformate (2.6 mL, 33.5 mmol) is added drop wise and the reaction mixture is allowed to stir for 15 hours and reach room temperature. The reaction mixture is separated with ether (3×50 mL), and the aqueous layer is contained in a round bottom flask and cooled over an ice-water bath. Concentrated HCl (aq) is added drop wise until pH 2. The reaction mixture is brought to room temperature and extracted with 2-Me-THF (3×50 mL). The organic layers are pooled, dried (MgSO4), the solids removed by filtration, and the solvents of the filtrate removed under reduced pressure. The compound was purified by silicagel chromatography with gradient elution from CH2Cl2 to CH2Cl2/MeOH/acetic acid 17/2/1. Fractions containing product were combined and the solvent were removed in vacuum, resulting in N-methoxycarbonyl-L-leucine (1.9 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433609B2
Source datasetuspto-grants-2016_09
ORD IDord-39ad65ac9fc142649a7bb14dd4f1e092
Source noteuspto-grants-2016_09