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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64645Generated: October 29, 2026

Iodine → 2-(4-Iodoethynylphenyl)-3-methyl-1-(1H-1,2,4-triazole-1-yl)butan-2-ol

https://huagongshe.com/reaction/64645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-ethynylphenyl)-3-methyl-1-(1H-1,2,4-triazole-1-yl)butan-2-olHCID 13473665—
SolventWaterHCID 962—
Product2-(4-Iodoethynylphenyl)-3-methyl-1-(1H-1,2,4-triazole-1-yl)butan-2-olHCID 13473700—

Reaction Steps

To a solution of 5.1 g 2-(4-ethynylphenyl)-3-methyl-1-(1H-1,2,4-triazole-1-yl)butan-2-ol in 100 ml abs. CH3OH are simultaneously added, with stirring at 20°-25°, 2.6 g iodine and 10 ml 30% NaOH solution. The reaction mixture is maintained at room temperature for 24 hours, with stirring, then poured into 500 ml H2O and extracted with CH2Cl2. The organic phase is washed, dried and evaporated. The residue is stirred in hexane fraction and kept over 16 hours at rest. The precipitate is sucked off and dried to give the title compound m.p. 122° as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609668
Source datasetuspto-grants-1986_09
ORD IDord-c31b3b7f96db41958ceae820174652c0
Source noteuspto-grants-1986_09