HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064535Generated: October 31, 2026
Water → 4-(4-chloro-benzylsulfanyl)-3,5-dimethyl-1H-pyrazole
https://huagongshe.com/reaction/1064535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 3-(4-Chloro-benzylsulfanyl)-pentane-2,4-dione | HCID 22174861 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-chloro-benzylsulfanyl)-3,5-dimethyl-1H-pyrazole | HCID 22174852 | 72% |
Reaction Steps
To a solution of crude 3-(4-chloro-benzylsulfanyl)-pentane-2,4-dione [prepared as described above from 3-chloro-pentan-2,3-dione (1.03 g, 7.63 mmol) and 4-chlorobenzyl mercaptan (1.21 g, 7.63 mmol)] in ethanol (60 mL) was added hydrazine hydrate (0.713 mL, 22.9 mmol) and p-toluenesulfonic acid monohydrate (ca. 25 mg). The solution was heated to reflux and stirred for 15 hours. The reaction mixture was allowed to cool to room temperature, and water (300 mL) was added. The precipitate that formed was removed by filtration, washed with water, and dried to provide 1.38 g (72%) of the product as a white solid: 1H NMR (CDCl3) δ 7.17 (d, J=8.4 Hz, 2H), 6.92 (d, J=8.4 Hz, 2H), 3.57 (s, 2H), and 2.02 (s, 6H) ppm. 13C NMR (CDCl3) δ 137.2, 132.7, 130.3, 128.3, 105.2, 39.9, 10.7 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969728B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-ec7d7be2470c43a9b4aca07b7b550a45 |
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| Source note | uspto-grants-2005_11 |
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