Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227837Generated: October 31, 2026

Methyl iodide → 3-Chloro-4-ethyl-6-phenylpyridazine

https://huagongshe.com/reaction/227837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3-Chloro-4-methyl-6-phenylpyridazineHCID 119999—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-ethyl-6-phenylpyridazineHCID 14450238—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A RBF was charged with 3-chloro-4-methyl-6-phenylpyridazine (5.0 g, 24 mmol) and 120 mL of THF under nitrogen, and the solution was cooled to −78° C. Lithium diisopropylamide, 2.0M in heptane/THF/ethylbenzene (15 ml, 29 mmol) was added and the mixture was stirred at −78° C. for 5 min, followed by RT for 1 h. The mixture was cooled to −78° C. and methyl iodide (1.8 ml, 29 mmol), which had been passed through a plug of basic alumina prior to use, was added dropwise. After stirring at −78° C. for 5 min, the reaction was stirred at RT for 0.5 h. Water was added to quench the reaction, and the mixture was concentrated and partitioned between dichloromethane and water. The layers were separated and the aqueous portion was extracted with additional DCM. The combined organics were dried with MgSO4, filtered and concentrated. The crude material was purified by silica gel chromatography (100% DCM to 95/5 DCM/MeOH) to provide 3-chloro-4-ethyl-6-phenylpyridazine as a tan solid. MS m/z=219 [M+H]+. Calc'd for C12H11ClN2: 218.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560551B2
Source datasetuspto-grants-2009_07
ORD IDord-f144ff9bbc9b446b983b94ea4941000b
Source noteuspto-grants-2009_07