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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721616Generated: November 3, 2026

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

https://huagongshe.com/reaction/1721616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantGlycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
ReactantUndec-4-eneHCID 136496—
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 g, 0.264 mol) in one portion. To the above clear solution added 74.94 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, a saturated sodium bicarbonate solution, and then 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 numberUS05512576
Source datasetuspto-grants-1996_04
ORD IDord-920aef5cd9684cc6be9ea361b41d332f
Source noteuspto-grants-1996_04