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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426514Generated: November 2, 2026

Acetaldehyde → 1-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-ethanol

https://huagongshe.com/reaction/2426514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant3-Methoxy-6-(pyridin-4-yl)pyridazineHCID 23092478—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-ethanolHCID 2309251666%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.93 g 2,2,6,6-tetramethylpiperidine in 30 ml THF is added 4.13 ml (15% solution in toluene) n-butyllithium at −30° C. After being stirred at 0° C. for 30 min, the reaction mixture is cooled to −78° C. and a solution of 1.12 g 3-methoxy-6-pyridin-4-yl-pyridazine in 30 ml THF is added and stirred at −78° C. for 30 min. At this temperature, 3.17 g acetaldehyde are added and stirred for another 2 h. The reaction is quenched by the addition of 24 ml MeOH/THF 1:1 and warmed to ambient temperature. Then, 30 ml saturated aq. NaHCO3 are added and extracted with CH2Cl2. The combined organic layers are washed with water, dried over MgSO4 and concentrated in vacuo. The residue is purified by flash chromatography (ethyl acetate 100%) to give 0.91 g (66%) of the desired product as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968546B2
Source datasetuspto-grants-2011_06
ORD IDord-9b432a5109844b018bce772305c3b5f4
Source noteuspto-grants-2011_06