Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Boc-N-methyl amino butanol | HCID 86759403 | — |
| Product | HCID 131055384 | HCID 131055384 | — |
Reaction Steps
The resulting N-Boc-N-methyl amino butanol (4.00 g) was placed in a 200-mL threeneck flask, and after nitrogen substitution, the compound was dissolved in 35 mL of anhydrous tetrahydrofuran. The solution was added with 60% sodium hydride (1.77 g), and stirred at room temperature for 30 minutes. Then, the reaction mixture was added dropwise with 1.87 mL of methyl iodide and stirred on an oil bath at 50° C. for 1.5 hours. The reaction was stopped with water, and the organic layer was extracted with ethyl acetate, washed once with water and once with saturated brine, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/4) to obtain 4.25 g of N-Boc-N-methyl-N-methoxybutylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713473B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-853bae317a1846ed85c68f0ebc01ad71 |
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| Source note | uspto-grants-2004_03 |
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