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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287319Generated: November 1, 2026

Methyl iodide → N-Cbz-N-methyl-L-leucine

https://huagongshe.com/reaction/2287319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantLeucine, N-carboxy-, N-benzyl ester, L-HCID 74840—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Cbz-N-methyl-L-leucineHCID 701055397.1%

Reaction Steps

To a solution of N-Cbz-leucine (1.38 g, 5.2 mmol) in THF (15 mL) at 0° C. was added methyl iodide (2.5 mL, 40.1 mmol). Sodium hydride (60% dispersion in oil, 0.6 g, 15 mmol) was added cautiously, and the resultant mixture was stirred at room temperature for 24 h. The reaction mixture was diluted with EtOAc (25 mL) and water (2 mL) was added dropwise. The mixture was concentrated to dryness, and the residue was partitioned between ether (15 mL) and water (50 mL). The organic layer was extracted with saturated aqueous NaHO3 (25 mL), and the combined aqueous extracts were acidified to pH 2 with 3N HCl. The product was extracted with EtOAc (3×25 mL), dried over MgSO4, filtered, and concentrated to afford the title compound (1.41 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083903
Source datasetuspto-grants-2000_07
ORD IDord-45832db20ff64741b072da1def22d752
Source noteuspto-grants-2000_07