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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083506Generated: November 1, 2026

Sulfuric Acid → HCID 20328055, compound

https://huagongshe.com/reaction/2083506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium PermanganateHCID 516875—
ReactantHCID 20327982HCID 20327982—
ReactantSodium BisulfiteHCID 23665763—
CatalystHCID 178418406HCID 178418406—
SolventWaterHCID 962—
ProductHCID 20328055HCID 20328055—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 3,4-dibromo-β-methylpyrazole-1-ethanol (2.8 g., 0.01 mole) prepared in Example 38, above, in sodium hydroxide (0.3 g., 0.0075 mole) and water (3.0 ml.), a solution of potassium permanganate (3.4 g., 0.0215 mole) in water (30 ml.) was added over a period of 20 minutes. A further 30 ml. of water was added and the reaction mixture was stirred at about 25° C. for 4 hours, followed by acidification with 6N sulfuric acid and addition of sodium bisulfite until all the precipitated manganese dioxide went into solution. The aqueous solution was extracted with three 50-ml. portions of ether and the combined ether extracts were washed with water and dried over anhydrous sodium sulfate. Evaporation of the ether under reduced pressure followed by chromatography on silica gel using the solvent system benzene, 85:chloroform, 5:glacial acetic acid, 10 (by volume) gave a solid which on recrystallization from acetone-hexane gave 3,4-dibromo-α-methylpyrazole-1-acetic acid having a melting point at 124.5° to 126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04084955
Source datasetuspto-grants-1978_04
ORD IDord-01f51a63829f4b268ea924ce67670c9b
Source noteuspto-grants-1978_04