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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Reactanttert-Butyl (3R)-3-benzoylpiperidine-1-carboxylateHCID 59382841—
ReactantLithim bis(trimethylsilylamide)HCID 86588160—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 3-benzoyl-3-methylpiperidine-1-carboxylateHCID 5938282465%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-aa1eca83947c4d8e848b02bc09532b10
Source noteuspto-grants-2013_06