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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982995Generated: October 28, 2026

Ethanol → HCID 178441177, compound

https://huagongshe.com/reaction/1982995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 86612676HCID 86612676—
SolventWaterHCID 962—
ProductHCID 178441177HCID 17844117742.6%

Reaction Steps

Under nitrogen atmosphere, mixture of 50.00 g of pinacolone and 42.00 g of methyl formate was cooled to 0° C., and then 56.00 g of potassium t-butoxide was added to the mixture over the period for 3 hours. During that, the temperature of the mixture was kept below 20° C. After that, the reaction mixture was stirred at 30° C. for 5 hours. Diethyl ether was added to the reaction mixture which was cooled to room temperature, as a result, solid was produced. The solid was collected by filtration, and dried under reduced pressure to give 32.12 g of 1-hydroxy-4,4-dimethyl-1-pentene-3-one potassium salt. 21.61 g of 1-hydroxy-4,4-dimethyl-1-pentene-3-one potassium salt was suspended to 150 ml of ethanol. 6.52 g of hydrazine hydrate was added to the suspension, and then refluxed for 7 hours. 50 ml of water was added to the reaction mixture which was cooled to room temperature, and the mixture was concentrated to 40 ml under reduced pressure. The concentrated solution was extracted by ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 6.83 g of 3-t-butyl-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541374B2
Source datasetuspto-grants-2009_06
ORD IDord-94cfbab794dd4f0c8073ac43b0712f7e
Source noteuspto-grants-2009_06