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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257734Generated: November 2, 2026

Hydrochloric Acid → 2-(2-Methoxyphenyl)-3-phenyl-2-[(1,2,4-triazol-1-yl)methyl]propanoic acid

https://huagongshe.com/reaction/257734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 20085199HCID 20085199—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-(2-Methoxyphenyl)-3-phenyl-2-[(1,2,4-triazol-1-yl)methyl]propanoic acidHCID 2008520057%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a clear solution of 3-benzyl-3-[(1,2,4-triazol-1-yl)methyl]-2(3H)-benzofuranone (11 g, 0.0360 mole) and methanol (100 mL), potassium hydroxide (45% solution) (0.5 g, 0.0750 mole) was added and the reaction mixture heated with stirring at reflux for 3 hours. The reaction mixture was then cooled to 25° C. and iodomethane (6.1 g, 0.0750 mole) added and the reaction mixture continued to stir at 50° C. for an additional 3 hours. The reaction solvent was then removed by distillation, and the residue stirred with hydrochloric acid (5 g, 0.37 mole) and 100 mL of water. The precipitated solid was filtered by suction and washed by 100 mL of hot ethyl acetate. The remaining solid was dried and gave 7.0 g, melting point 250°-252° C. (yield 57%), Example 95 of Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264415
Source datasetuspto-grants-1993_11
ORD IDord-f33df4bd97104946bd15ad831c9f6574
Source noteuspto-grants-1993_11