HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725116Generated: November 2, 2026
Hydrochloric Acid → HCID 178527394, compound
https://huagongshe.com/reaction/1725116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzenesulfinic acid, sodium salt | HCID 2723840 | — |
| Reactant | HCID 178516151 | HCID 178516151 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178527394 | HCID 178527394 | 88.1% |
Reaction Steps
5-Hydroxy-1-phenyl-3-trifluoromethylpyrazole (2.3 g (10 mmol)) synthesized in Reference Example 2 and 0.6 g (15 mmol) of sodium hydroxide were dissolved in 10 mL of water. While stirring the resulting solution at room temperature, 1.7 g (20 mmol) of a 35% formalin solution was added dropwise thereto, followed by stirring at the same temperature for 1 hour. Subsequently, 1.6 g (10 mmol) of sodium benzenesulfinate was charged thereto at room temperature, and the obtained mixture was stirred for 2 hours. After the reaction, 6.0 g (60 mmol) of 35% hydrochloric acid was added dropwise thereto, and the toluene layer obtained from an extraction operation performed twice with 20 mL of toluene was washed with 10 mL of water and then with 10 mL of saturated brine and dried over anhydrous sodium sulfate. Thereafter, toluene was removed by distillation under reduced pressure to obtain 3.4 g (yield: 88.1%) of the title compound as a viscous material. This viscous material was left standing at room temperature for 2 days and thereby crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488831B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-6103c74737834fea84d9f98c10dc4236 |
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| Source note | uspto-grants-2009_02 |
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