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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576253Generated: November 2, 2026

Water → 3,5-Diphenyl-1-(prop-2-en-1-yl)-4-propoxy-1H-pyrazole

https://huagongshe.com/reaction/1576253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
Reactant3,5-Diphenyl-4-propoxy-1H-pyrazoleHCID 21398099—
ReactantPotassium tert-butoxideHCID 23665647—
SolventIsopropanolHCID 3776—
Product3,5-Diphenyl-1-(prop-2-en-1-yl)-4-propoxy-1H-pyrazoleHCID 2151447255%

Reaction Conditions

Temperature50 °C

Reaction Steps

3,5-Diphenyl-4-n-propoxypyrazole (9.0 g, 0.038 mole) is dissolved in 2-propanol (90 ml). Potassium t-butoxide (4.65 g, 0.042 mole) is added at room temperature and the reaction mixture stirred and heated at 50°C for 3 hours. It is then cooled to room temperature and 3-bromoprop-1-ene (5.53 g, 0.046 mole) is added dropwise. A white solid forms. Stirring is continued at room temperature overnight, the mixture is then poured into water and extracted with chloroform. The chloroform layer is washed with water (3 × 150 ml) and stripped under vacuum. The residual oil is purified by dry column chromatography (silica gel/toluene). The toluene solution is stripped under vacuum to afford 6.64 g (55%) product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979409
Source datasetuspto-grants-1976_09
ORD IDord-4000302488814b80a6872da428834eab
Source noteuspto-grants-1976_09