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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450459Generated: October 31, 2026

Methyl iodide → Methyl N-(tert-butoxycarbonyl)-N-methylglycinate

https://huagongshe.com/reaction/1450459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantGlycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
SolventBenzeneHCID 241—
ProductMethyl N-(tert-butoxycarbonyl)-N-methylglycinateHCID 1401893086.4%

Reaction Steps

To a solution of N-t-butoxycarbonyl-sarcosine (50 g; 0.264 mol) in 700 ml of benzene was added 1,8-diazabicyclo[5.4.0]-undec-7-ene (DBU; 40.19, 0.264 mol) in one portion. To the above clear solution was added 74.84 g (0.528 mol) of methyl iodide in one portion and the resulting clear solution was allowed to reflux for 7 hours. After adding additional methyl iodide (16 ml), the reaction mixture was refluxed with stirring and then cooled to room temperature, and stirred overnight. The reaction mixture was filtered, the residue washed with ether, and the combined filtrate was washed with water, saturated sodium bicarbonate solution, and brine. The resulting organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to afford 46.38 g (86.4%) of N-t-butoxycarbonyl-sarcosine methyl ester as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602154
Source datasetuspto-grants-1997_02
ORD IDord-17700ac8debc4dc0aea5238b9fe283af
Source noteuspto-grants-1997_02