Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212086Generated: November 2, 2026

Methyl iodide → HCID 69663221, compound

https://huagongshe.com/reaction/2212086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 69663224HCID 69663224—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69663221HCID 69663221—

Reaction Steps

A solution of n-butyllithium (1.5M, 0.13 ml, 0.2 mmol) in hexanes was added to a stirred solution of 1-(4-benzenesulfonyl-3,3-dimethyl-butyl)-4-trifluoromethylpiperidine (40 mg, 0.11 mmol) in tetrahydrofuran (2 ml) at −78° C. The mixture was stirred for 30 min. and methyl iodide (0.34 ml) was added. After 1 hour, the reaction mixture was quenched with one drop of water and concentrated in vacuo. The residue was purified on silica gel (dichloromethane:methanol) to give 1-(4-benzenesulfonyl-3,3-dimethyl-pentyl)-4-trifluoromethyl-piperidine. The title product was prepared by treatment of the amine with 1M ethereal HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101892B2
Source datasetuspto-grants-2006_09
ORD IDord-ed4b764ad15c48a0ac2592b9ae6aef42
Source noteuspto-grants-2006_09