HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422355Generated: October 29, 2026
2-Methylquinoline → 2-(4-Trimethylsilanyl-but-3-ynyl)-quinoline
https://huagongshe.com/reaction/422355
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylquinoline | HCID 7060 | — |
| Reactant | 3-Bromo-1-(trimethylsilyl)-1-propyne | HCID 642589 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Trimethylsilanyl-but-3-ynyl)-quinoline | HCID 66598438 | 64% |
Reaction Steps
2-Methyl-quinoline (0.28 mL, 2.09 mmol) was added dropwise to a solution of LDA (3.0 mL, 0.8 M in THF) in THF (3 mL) at −78° C. and the reaction mixture was stirred for 1 hour at −78° C. Then (3-bromo-prop-1-ynyl)-trimethyl-silane (0.39 mL, 2.51 mmol) was added to the reaction mixture, the solution was stirred for 18 hours at room temperature and was quenched with water. The aqueous phase was extracted with DCM. The organic phase was washed with water, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 9:1) to yield 338 mg (1.33 mmol, 64%) of 2-(4-trimethylsilanyl-but-3-ynyl)-quinoline as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101637B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3c651f8445aa49279d7c6c5346361ebe |
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| Source note | uspto-grants-2012_01 |
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