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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52780Generated: October 30, 2026

Tetramethyltin → 4-Methoxy-3-methyl-6-[3-(trifluoromethyl)phenyl]pyridazine

https://huagongshe.com/reaction/52780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
Reactant3-Bromo-4-methoxy-6-[3-(trifluoromethyl)phenyl]pyridazineHCID 19959669—
CatalystPalladium(2+) chloride phenylmethanide--triphenylphosphane (1/1/1/2)HCID 11007180—
SolventDimethylformamideHCID 6228—
Product4-Methoxy-3-methyl-6-[3-(trifluoromethyl)phenyl]pyridazineHCID 1995968063%

Reaction Steps

3-Bromo-4-methoxy-6-[3-(trifluoromethyl)phenyl]pyridazine (1.0 g, 0.003 mole, Compound No. 65), tetramethyltin (1.28 g, 0.0072 mole) and trans-benzyl(chloro)bis-(triphenylphosphine)palladium(II) (20 mg) were heated to 100° C. in DMF under N2 for 18 h. The reaction was then cooled and partitioned between aqueous KF solution and ethyl acetate. The KF solution was extracted with additional ethyl acetate. The organic layers were washed with brine, dried (MgSO4), filtered through silica gel and then evaporated in vacuo. The crude oil was then chromatographed on a Prep-500 to give 4-methoxy-3-methyl-6-[3-(trifluoromethyl)phenyl]pyridazine (0.51 g, 63% yield, Compound No. 66) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616789
Source datasetuspto-grants-1997_04
ORD IDord-2ab40c400534466385ccf8fc97961d12
Source noteuspto-grants-1997_04