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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030979Generated: October 30, 2026

Sulfuric Acid → HCID 19025451, compound

https://huagongshe.com/reaction/1030979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantHCID 19025437HCID 19025437—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 19025451HCID 1902545136.8%

Reaction Steps

To a stirred, warm (40° C.) solution of 10.8 g (0.0648 mole) of potassium iodide in 80 ml of water was added dropwise a solution of 10.0 g (0.0324 mole) of 4-(4-amino-2-chlorophenyl)-3-trifluoromethyl-4,5-dihydro-1-methyl-1,2,4-triazol-5(1H)-thione (Compound 94 of Table 1, prepared in Step C of Example 2), 2.70 g (0.389 mole) of sodium nitrite, and 20.0 g (0.204 mole) of concentrated sulfuric acid in 125 g of ice-cold water. The resultant mixture was stirred at 40° C. for three hours. The mixture was cooled and was extracted with methylene chloride. The extract was washed with an aqueous sodium metabisulfite solution. The washed organic phase was dried over anhydrous magnesium sulfate and was filtered. The filtrate was evaporated under reduced pressure, leaving a residue. This residue was purified by column chromatography on silica gel, eluting with petroleum ether:diethyl ether (75:25) to yield 5.0 g of 4-(2-chloro-4-iodophenyl)-3-trifluoromethyl-4,5-dihydro-1-methyl-1,2,4-triazol-5(1H)-thione as a solid, mp 117°-119° C., Compound 91 of Table 1. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05108486
Source datasetuspto-grants-1992_04
ORD IDord-ca7f830f600a4b28a097ebdcdadf7ba3
Source noteuspto-grants-1992_04