Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042425Generated: October 29, 2026

Methyl iodide → methyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninate

https://huagongshe.com/reaction/1042425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-((tert-Butoxycarbonyl)(2-cyanoethyl)amino)-2-methylpropanoic acidHCID 57523644—
SolventDimethylformamideHCID 6228—
Productmethyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninateHCID 5752364597%

Reaction Steps

62 g (0.23 mol) of N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalanine were dissolved in 350 ml of DMF and 50 g of KHCO3 were added. Few minutes after, 30 ml of methyl iodide (MeI) were dropped and the mixture was stirred at room temperature for 6 hours. Then a further 15 ml of MeI were added. The mixture was left at room temperature overnight. After dilution with 1.5 l of water, the solution was extracted with ethyl acetate (3 times). The organic phases were washed with a small amount of water, dried over sodium sulfate, evaporated and dried at the mechanical pump. 60.5 g (97%) of methyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninate were thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557857B2
Source datasetuspto-grants-2013_10
ORD IDord-dd59f248017346a78a5105b9afae474a
Source noteuspto-grants-2013_10