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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624054Generated: November 2, 2026

Hydrazinium chloride → HCID 178426391, compound

https://huagongshe.com/reaction/1624054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinium chlorideHCID 115031—
ReactantHCID 71114823HCID 71114823—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 178426391HCID 178426391—

Reaction Conditions

Temperature80 °C

Reaction Steps

Hydrazine hydrochloride (0.14 g, 2 mmol) is added to 4-[(2Z)-2-(dimethylaminomethylene)-4,4-dimethyl-3-oxo-cyclohexyl]-3-methyl-benzonitrile (0.2 g, 0.67 mmol) in ethanol (30 mL), then acetic acid (two drops) is added to the mixture. After the addition is complete, the reaction mixture is stirred at 80° C. for 3 h. The mixture is cooled to room temperature and concentrated in vacuo. The residue is diluted with ethyl acetate (50 mL) and saturated sodium bicarbonate solution (50 mL). The organic phase is separated and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phase is washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography (eluted with pet ether:EtOAc=2:1 to 1:1) to give the title compound. The product is added to HCl/ethyl acetate and concentrated in vacuo to give the HCl salt of the title compound (0.12 g, 67%). ES/MS 266 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778984B2
Source datasetuspto-grants-2014_07
ORD IDord-67a5d19738b74ac090cffd9b7865c43f
Source noteuspto-grants-2014_07