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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410382Generated: November 2, 2026

Water → 4-(4-chloro-benzylsulfanyl)-3,5-dimethyl-1H-pyrazole

https://huagongshe.com/reaction/1410382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant3-(4-Chloro-benzylsulfanyl)-pentane-2,4-dioneHCID 22174861—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthanolHCID 702—
Product4-(4-chloro-benzylsulfanyl)-3,5-dimethyl-1H-pyrazoleHCID 2217485272%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921547B2
Source datasetuspto-grants-2014_12
ORD IDord-e4fec1d6d6e342ea9aa6735f4981345d
Source noteuspto-grants-2014_12