HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736321Generated: October 30, 2026
Methyl iodide → Methyl N-(tert-butoxycarbonyl)-N-methylglycinate
https://huagongshe.com/reaction/1736321
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl- | HCID 83692 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl N-(tert-butoxycarbonyl)-N-methylglycinate | HCID 14018930 | 86.4% |
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 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05541168 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-25d52389f85a44ebbeb4261fa8af7642 |
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| Source note | uspto-grants-1996_07 |
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