HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254191Generated: October 25, 2026
Methyl iodide → Tert-butyl 3-benzoyl-3-methylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1254191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Reactant | tert-Butyl (3R)-3-benzoylpiperidine-1-carboxylate | HCID 59382841 | — |
| Reactant | Lithim bis(trimethylsilylamide) | HCID 86588160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Tert-butyl 3-benzoyl-3-methylpiperidine-1-carboxylate | HCID 59382824 | 65% |
Reaction Steps
A stirred solution of (R)-tert-butyl 3-benzoylpiperidine-1-carboxylate (409 mg, 1.42 mmol) in dry THF (15 mL) under N2 was cooled to −78° C. A solution of lithium bis(trimethylsilylamide) in THF (2.84 mL of 1.0M, 2.84 mmol, 2 equiv) was added dropwise. After 30 min, a solution of iodomethane (220 μL, 3.5 mmol, 2.5 equiv) in DMPU (512 μL, 4.24 mmol, 3.0 equiv) was added slowly. After 15 min, the reaction mixture was allowed to warm to rt and stirred overnight. LC-MS showed the reaction was complete. Brine (50 mL) was added to quench the reaction. The organic layer was separated and the aqueous layer was extracted with EtOAc (2×75 mL). The combined organic layers were dried over Na2SO4. After concentration, the crude product was purified by chromatography on a prepacked 12-g silica gel cartridge eluted with a 0-35% EtOAc in hexanes gradient to afford tert-butyl 3-benzoyl-3-methylpiperidine-1-carboxylate (278 mg, 65%). LC-MS (3 min) tR=1.92 min, m/z 326 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455521B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-aa1eca83947c4d8e848b02bc09532b10 |
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| Source note | uspto-grants-2013_06 |
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