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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 3,5-Diphenyl-4-propoxy-1H-pyrazole | HCID 21398099 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3,5-Diphenyl-1-(prop-2-en-1-yl)-4-propoxy-1H-pyrazole | HCID 21514472 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03979409 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-4000302488814b80a6872da428834eab |
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| Source note | uspto-grants-1976_09 |
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