Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750725Generated: November 3, 2026

Methyl iodide → Ethyl 4-(4-(cyclohexylmethyl)-4-methoxypiperidin-1-yl)benzoate

https://huagongshe.com/reaction/1750725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-(4-(cyclohexylmethyl)-4-hydroxypiperidin-1-yl)benzoateHCID 16109048—
SolventTetrahydrofuranHCID 8028—
SolventSodium BisulfateHCID 516919—
ProductEthyl 4-(4-(cyclohexylmethyl)-4-methoxypiperidin-1-yl)benzoateHCID 16109132—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of Example 1F (380 mg) in THF (5 mL) was treated with NaH (96 mg, 60% dispersion in mineral oil), heated to 50° C. for 2 hours, and treated with hexamethylphosphoramide (1 mL) followed by MeI (1 mL). The reaction mixture was refluxed overnight, cooled to 0° C., and diluted with saturated aqueous NaHSO4 solution (10 mL). The resulting two-phase mixture was separated, the aqueous phase was extracted twice with ether, and the combined organic layers washed with water and brine. After drying over MgSO4, the mixture was concentrated in vacuo and purified by silica gel chromatography eluting with 15% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156856B2
Source datasetuspto-grants-2015_10
ORD IDord-7d7f6722ea8647de8788777455c9b1cc
Source noteuspto-grants-2015_10