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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643566Generated: October 30, 2026

Methyl iodide → Tert-butyl 4-[3-(benzyloxy)-2-methyl-3-oxopropyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/643566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTert-butyl 4-[3-(benzyloxy)-3-oxopropyl]piperidine-1-carboxylateHCID 59261015—
ReactantLDA cyclohexaneHCID 86604122—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-[3-(benzyloxy)-2-methyl-3-oxopropyl]piperidine-1-carboxylateHCID 59261045—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled (−78° C.) solution of 1.5M LDA/cyclohexane (6.48 mL, 9.73 mmol) in 50 mL of THF was added dropwise under a nitrogen atmosphere a solution of tert-butyl 4-[3-(benzyloxy)-3-oxopropyl]piperidine-1-carboxylate (2.60 g, 7.48 mmol) in 20 mL of THF. The resulting mixture was stirred at −78° C. for 45 min then was treated dropwise with neat iodomethane (1.40 mL, 22.4 mmol). After stirring at −78° C. for an additional 30 min, the reaction mixture was permitted to warm to rt and stir overnight. The reaction mixture was diluted with ether and washed in sequence with 1N HCl solution, saturated NaHCO3 solution, and brine. The ethereal layer was dried over anhydrous MgSO4, filtered, and concentrated. Purification by MPLC (silica, 25% ethyl acetate/hexanes) afforded tert-butyl 4-[3-(benzyloxy)-2-methyl-3-oxopropyl]piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700591B2
Source datasetuspto-grants-2010_04
ORD IDord-ec997150e3c04227be761494aad27571
Source noteuspto-grants-2010_04