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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816358Generated: October 26, 2026

Methyl iodide → Tert-butyl 4-cyclohexyl-4-methoxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/1816358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-cyclohexyl-4-hydroxypiperidine-1-carboxylateHCID 22492872—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-cyclohexyl-4-methoxy-1-piperidinecarboxylateHCID 22492894—

Reaction Steps

To a solution of tert-butyl 4-cyclohexyl-4-hydroxy-1-piperidinecarboxylate (7.26 g) in DMF (70 ml) was added sodium hydride (60% in oil) (2.05 g) with stirring under ice-cooling. The mixture was stirred at ambient temperature for 1 hour. To the suspension was added methyl iodide (4.79 ml) and the mixture was stirred at ambient temperature overnight. The reaction mixture was poured into ice-water (300 ml) and extracted three times with ethyl acetate (200 ml). The extracts were collected, washed twice with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The resulting residue was chromatographed on silica gel (400 ml) eluting with a mixture of n-hexane and ethyl acetate (4:1 v/v). The fractions containing the desired compound were collected and evaporated under reduced pressure to give tert-butyl 4-cyclohexyl-4-methoxy-1-piperidinecarboxylate (6.77 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884774B2
Source datasetuspto-grants-2005_04
ORD IDord-1a48c849a52449c2acdc3931cf01c0b7
Source noteuspto-grants-2005_04