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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731717Generated: November 4, 2026

Ammonium Hydroxide → Pyridazine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-

https://huagongshe.com/reaction/1731717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 12449558HCID 12449558—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductPyridazine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 1065754278.5%

Reaction Steps

To 3-chloro-4-methyl-6-(α,α,α-trifluoro-m-tolyl)pyridazine(7 g) is added 10% palladium on carbon catalyst (0.7 g) and 300 mL of MeOH containing 30 mL of concentrated NH4OH. The mixture is shaken with H2 until the uptake of H2 ceases. The mixture is filtered to remove catalyst and concentrated in vacuo and then diluted with CH2Cl2 /H2O. The organic phase is washed with water and dried over MgSO4 to yield a solid which, on recrystallization from Et2O, gives 4.8 g (78%) of an off-white solid with a melting point of 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623376
Source datasetuspto-grants-1986_11
ORD IDord-7780728892704690a50f601a94727f4b
Source noteuspto-grants-1986_11