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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940122Generated: October 25, 2026

Methyl iodide → N-(tert-Butoxycarbonyl)-N-methyl-D-alanine

https://huagongshe.com/reaction/1940122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantBOC-D-alanineHCID 637606—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-Butoxycarbonyl)-N-methyl-D-alanineHCID 16211306—

Reaction Steps

To 48 ml of a solution of Boc-D -Ala-OH (3.0 g, 15.9 mmol) in tetrahydrofuran (THF) was added 60% sodium hydride (1.9 g, 47.6 mmol) under ice-cooling and the mixture was stirred for 10 minutes. Then, methyl iodide (7.9 ml, 127 mmol) was added and the mixture was further stirred at room temperature for 22 hours. The reaction mixture was then concentrated under reduced pressure, ice-cooled, acidified with 10% citric acid-H2O, and extracted with ethyl acetate. The extract was washed with saturated NaCl-H2O, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was crystallized from hexane and the crystal crop was washed with hexane to provide the title compound. Yield 3.07 g (94.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698670
Source datasetuspto-grants-1997_12
ORD IDord-b8bc3247e8784172a873f1c3fe794e9a
Source noteuspto-grants-1997_12