HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686069Generated: October 26, 2026
Lithium diisopropylamide → 2-Chloro-3-(2,2-dipyridin-3-ylethyl)pyridine
https://huagongshe.com/reaction/1686069
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 3,3'-Methylenedipyridine | HCID 14762640 | — |
| Reactant | 3-(Bromomethyl)-2-chloropyridine | HCID 18931028 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-3-(2,2-dipyridin-3-ylethyl)pyridine | HCID 86634319 | — |
Reaction Steps
A solution of bis-(3-pyridyl)methane in 150 mL of THF was cooled to −30 C. LDA (1.5 M solution in cyclohexane, 29.4 mL) was added dropwise to give a dark red solution containing some red solid matter. The mixture was then stirred at 0 C for 10 min. A solution of 3-(bromomethyl)-2-chloropyridine in 50 mL of THF was added dropwise over 25 min, and the reaction was stirred at 0 C for 2 h, after which the reaction was quenched by adding saturated aqueous NH4Cl. The mixture was partitioned between saturated aqueous sodium bicarbonate and CH2Cl2. The aqueous solution was extracted with CH2Cl2 (3×), and the combined organic solutions were dried (Na2SO4) and concentrated. Flash chromatography gave 9.1 g of 2-chloro-3-(2,2-dipyridin-3-ylethyl)pyridine as a red, viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148535B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-aa795bb8d0104db68904c84d988e479a |
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| Source note | uspto-grants-2012_04 |
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