HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012241Generated: October 27, 2026
Water → tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1012241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylate | HCID 1514447 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate | HCID 58826553 | 105.6% |
Reaction Steps
To a solution of tert-butyl (R)-3-hydroxymethylpiperidine-1-carboxylate (11.50 g, 53.7 mmol) in N,N-dimethylformamide (110 ml) was added sodium hydride (3.22 g, 80.6 mmol) under ice-cooling, and the mixture was stirred at room temperature for 20 min. To the reaction mixture was added methyl iodide (4.35 ml, 69.9 mmol) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate (13.00 g, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977331B1 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-fa25481f88784feda7f968545fdab1df |
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| Source note | uspto-grants-2011_07 |
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