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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725116Generated: November 2, 2026

Hydrochloric Acid → HCID 178527394, compound

https://huagongshe.com/reaction/1725116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenesulfinic acid, sodium saltHCID 2723840—
ReactantHCID 178516151HCID 178516151—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178527394HCID 17852739488.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488831B2
Source datasetuspto-grants-2009_02
ORD IDord-6103c74737834fea84d9f98c10dc4236
Source noteuspto-grants-2009_02