HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196747Generated: November 1, 2026
Methyl iodide → Ethyl 4-(4-(cyclohexylmethyl)-4-methoxypiperidin-1-yl)benzoate
https://huagongshe.com/reaction/2196747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-(4-(cyclohexylmethyl)-4-hydroxypiperidin-1-yl)benzoate | HCID 16109048 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Bisulfate | HCID 516919 | — |
| Product | Ethyl 4-(4-(cyclohexylmethyl)-4-methoxypiperidin-1-yl)benzoate | HCID 16109132 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338466B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-65e68a647f4348559d8f08a1b3b60c0e |
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| Source note | uspto-grants-2012_12 |
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