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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359284Generated: November 2, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 131723994, compound

https://huagongshe.com/reaction/1359284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantPyridazineHCID 9259—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 131723994HCID 131723994—

Reaction Conditions

Temperature0 °C

Reaction Steps

11.2 ml of a hexane solution containing 2.52 mol of n-butyllithium was slowly added to a solution of 30 ml of tetrahydrofuran containing 4.8 ml of 2,2,6,6-tetramethylpiperidine at −30° C., followed by stirring at 0° C. for 30 minutes. Thereafter, 7.3 ml of N,N,N′,N′-tetramethylethylenediamine was added and then a mixture of 1.74 ml of pyridazine, 10.3 ml of tri-n-butyltin chloride and 10 ml of tetrahydrofuran was slowly added to the mixture at −78° C., followed by stirring at −78° C. for 3 hours, Then, water was added to the reaction solution, and then extracted with ethyl acetate. The organic phase was washed with brine and the solvent was removed. Then, the residue was subjected to NH-silica gel (Fuji Silicia) column chromatography and eluted with hexane/ethyl acetate (10:1), and then subjected to silica gel chromatography and eluted with hexane/ethyl acetate (10:1) and then with hexane/ethyl acetate (1:1), to give 660 mg of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-b3dd563a29234fa0ae25e8f2af2a18f8
Source noteuspto-grants-2003_07