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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524912Generated: October 30, 2026

Methyl iodide → Tert-butyl 4-methyl-4-(methylthio)piperidine-1-carboxylate

https://huagongshe.com/reaction/524912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl 4-mercapto-4-methylpiperidine-1-carboxylateHCID 71629631—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-methyl-4-(methylthio)piperidine-1-carboxylateHCID 8672096596.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-methyl-4-sulfanyl-piperidine-1-carboxylate (380 mg, 1.642 mmol) in THF (5 mL) cooled to −78° C. was added LiHMDS (1.724 mL of 1 M, 1.724 mmol) and the solution stirred for 10 mins before MeI (256.3 mg, 0.1124 mL, 1.806 mmol) was added and the solution allowed to warm to 0° C. over approximately 1 h. The reaction was then quenched carefully by the addition of saturated ammonium chloride and extracted into EtOAc. The aqueous was further extracted with EtOAc and the combined organics were washed with brine, dried (MgSO4) and concentrated to give a yellow oil (390 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-459917c0919c488ea286fe7c65a8439b
Source noteuspto-grants-2016_05