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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372764Generated: November 3, 2026

Methyl iodide → HCID 15096756, compound

https://huagongshe.com/reaction/2372764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyl-4,4-dimethoxypiperidin-3-olHCID 3019274—
SolventDimethylformamideHCID 6228—
ProductHCID 15096756HCID 1509675664.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-Phenylmethyl-3-hydroxy-4,4-dimethoxypiperidine (3b, 5.5g, 22 mmol) from Example 1 in 30ml of dimethylformamide was added slowly to a stirred suspension of sodium hydride (0.81g, 27 mmol, 80% oil suspension) in 100ml of dimethylformamide. The reaction mixture was warmed to 60° C. for 2 hours, then cooled to 0° C. whereupon methyl iodide (3.8g, 27 mmol) was slowly added to the mixture. The reaction mixture was stirred overnight at room temperature then quenched with 10ml of 10% sodium hydroxide solution. The reaction mixture was concentrated under vacuum, the residue slurried in 300ml of water and the aqueous mixture extracted with 3×100ml of ether. The combined organic layers were dried over magnesium sulfate, concentrated under vacuum, then purified by column chromatography (alumina; ethyl acetate/hexane; 2.5:1) to yield the intermediate 1-phenylmethyl-3-methoxy-4,4-dimethoxypiperidine (4b, 3.77g, 64.6%, Rf 0.63).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100903
Source datasetuspto-grants-1992_03
ORD IDord-6fc36123d25840edbe7287ac4c58f4ca
Source noteuspto-grants-1992_03