HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293845Generated: October 31, 2026
HCID 21471327, compound → HCID 11066164, compound
https://huagongshe.com/reaction/2293845
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 21471327 | HCID 21471327 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11066164 | HCID 11066164 | 73% |
Reaction Steps
A solution of 3-(2,2-dibromoethenyl)-2-(4-fluorophenyl)-4-(1-methylethyl)quinoline (2.563 gm, 5.71 mmol) in dry THF (30 ml) was cooled to -78° C. and treated with n-BuLi (1.5M in hexane, 8.0 ml, 12 mmol) over a 5 minute period. After stirring at -78° C. for 1.25 hours, the brown solution was quenched with saturated NH4Cl, warmed to room temperature, diluted with H2O, and extracted 2× with Et2 O. The combined Et2O extracts were washed with brine, dried (Na2SO4), filtered and stripped to give a yellow solid. The solid was recrystallized from hot hexane to afford analytically pure 3-ethynyl-2-(4-fluorophenyl)-4-(1-methylethyl)quinoline as off-white crystals (1.205 gm, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686433 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-0f82e7428a9f4b18ba2bd64312bf2f63 |
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| Source note | uspto-grants-1997_11 |
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