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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22597Generated: October 25, 2026

Trimethylsulfonium iodide → 2-(3-(2-(7-Chloroquinolin-2-yl)cyclopropyl)phenyl)1,3-dioxolane

https://huagongshe.com/reaction/22597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant2-(3-(2-(7-Chloroquinolin-2-yl)ethenyl)phenyl)-1,3-dioxolaneHCID 53685324—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(3-(2-(7-Chloroquinolin-2-yl)cyclopropyl)phenyl)1,3-dioxolaneHCID 10405721—

Reaction Conditions

Temperature21 °C

Reaction Steps

To a solution of trimethylsulfonium iodide (2.128 g, 10.4 mmoles) in 20 mL of anhydrous THF at -10° C. was added dropwise a solution of n-butyllithium 1.6M in hexanes (4.9 mL, 0.75 equiv.). Then the temperature was raised to 21° C. for 2 hours. To this mixture cooled to 0° C., the alkene (step 2) (967 mg, 2.86 mmoles) in 5 mL THF was added and the solution stirred overnight. Hydrolysis with 25% aqueous NH4OAc, extraction with EtOAc and flash chromatography on silica using EtOAc:toluene 2.5:97.5 afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428171
Source datasetuspto-grants-1995_06
ORD IDord-c503a7df0f134bb2832625ca3ad201ea
Source noteuspto-grants-1995_06