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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099349Generated: October 26, 2026

Hydrazine hydrate (1:1) → 4-(7-Methoxy-indan-4-yloxy)-3,5-dimethyl-1H-pyrazole

https://huagongshe.com/reaction/1099349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-2,4-pentanedioneHCID 74328—
ReactantPotassium BromideHCID 253877—
Reactant7-methoxy-2,3-dihydro-1H-inden-4-olHCID 20609156—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(7-Methoxy-indan-4-yloxy)-3,5-dimethyl-1H-pyrazoleHCID 6681246618.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To the suspension of 60% Sodium hydride (2.0 gm, 0.051 moles) in Tetrahydrofuran (20 ml) added a solution of 7-Methoxyindan-4-ol (7.0 gm, 0.042 mole) in Tetrahydrofuran (30 ml) at room temperature. After one hour stirring a solution of 3-Chloro 2,4-pentanedione (9.0 ml, 0.075 mole) in Tetrahydrofuran (20 ml) was added followed by addition of Potassium bromide (3.0 gm, 0.025 mole). The reaction mixture was stirred at 70° C. for 6 hours. The water was added and extracted with Diethyl ether. The Ether layer was separated and distilled off to give an oily mass which was partially purified through a column using 2% Ethyl acetate in Hexane to give crude mass (2.7 gm). The obtained crude mass was stirred with Hydrazine hydrate (1 ml) in 20 ml Ethanol at 10° C. Ethanol was evaporated to dryness. The obtained residue was partitioned between water and Ethyl acetate. The separated Ethyl acetate layer was dried over Sodium sulphate and distilled off to give desired product (2.0 gm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143424B2
Source datasetuspto-grants-2012_03
ORD IDord-67998dc8459f4f48b819aa84291223e6
Source noteuspto-grants-2012_03