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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503424Generated: October 25, 2026

Lithium diisopropylamide → 1-(Pyridazin-3-yl)ethan-1-ol

https://huagongshe.com/reaction/1503424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
Reactant6'-Bromospiro[cyclohexane-1,2'-indene]-1',4(3'H)-dioneHCID 58197205—
ReactantN-methoxy-N-methylpyridazine-3-carboxamideHCID 58197546—
SolventTetrahydrofuranHCID 8028—
Product1-(Pyridazin-3-yl)ethan-1-olHCID 15197511106.6%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of LDA (23.4 mL, 42.1 mmol, 1.8 M in THF) in THF (150 mL) was added slowly a solution of compound 1 (3.6 g, 21.05 mmol) in THF (77 mL) at −60° C. under a N2 atmosphere. After being stirred at −60° C. for 1 h, a solution of compound 2 (7.05 g, 18.9 mmol)) in THF (23 mL) was added slowly to the above solution. The resulting mixture was stirred at −60° C. for 2 h. The reaction mixture was quenched with water (15 mL). The aqueous layer was extracted with EtOAc (3×40 mL). The combined organic layers were washed with brine (20 mL), dried over Na2SO4 and concentrated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel (petroleum:ethyl acetate, 10:1) to give compound 3 (2.5 g, yield 26%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212153B2
Source datasetuspto-grants-2015_12
ORD IDord-7734bd19058340a4acf9a5ea71277674
Source noteuspto-grants-2015_12