HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 4-(((tert-butoxycarbonyl)(methyl)amino)methyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-((((1,1-dimethylethoxy)carbonyl)amino)methyl)benzoate | HCID 14221817 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(((tert-butoxycarbonyl)(methyl)amino)methyl)benzoate | HCID 17789107 | 94% |
Reaction Steps
To a solution of methyl 4-[[(tert-butoxycarbonyl)amino]methyl]benzoate (compound obtained in Reference Example 81(1), 2.0 g) in tetrahydrofuran (20 mL) is added sodium hydride (60% dispersion in mineral oil, 0.9 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes and then to the reaction mixture is added dropwise methyl iodide (2.3 mL). The mixture is stirred at room temperature for 3 hours. The reaction mixture is diluted with ethyl acetate, washed with water, and concentrated in vacuo to give methyl 4-[[N-methyl-N-(tert-butoxycarbonyl)amino]-methyl]benzoate (1.9 g, yield; 94%) as a yellow oil. MS (APCI) m/z: 280 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384952B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-307dbef7c4144e9681d165ff89ba1cfc |
| Source note | uspto-grants-2008_06 |