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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | 2-(3-(2-(7-Chloroquinolin-2-yl)ethenyl)phenyl)-1,3-dioxolane | HCID 53685324 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-(2-(7-Chloroquinolin-2-yl)cyclopropyl)phenyl)1,3-dioxolane | HCID 10405721 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428171 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-c503a7df0f134bb2832625ca3ad201ea |
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| Source note | uspto-grants-1995_06 |
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