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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566244Generated: October 30, 2026

Trityl chloride → Ethyl (1-triphenylmethyl-1H-1,2,4-triazol-3-yl)acetate

https://huagongshe.com/reaction/566244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 178470784HCID 178470784—
SolventDimethylformamideHCID 6228—
ProductEthyl (1-triphenylmethyl-1H-1,2,4-triazol-3-yl)acetateHCID 5436105935.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl (1H-1,2,4-triazol-3-yl)acetate (2.83 g) was dissolved in DMF (40 ml). To the solution were added triphenyl methyl chloride (5.08 g) and triethylamine (2.55 ml). The mixture was stirred for 3 hours at 25° C. The reaction mixture was added to ice-water (150 ml), which was subjected to extraction with ethyl ether (100 ml). The organic layer was washed twice with water (150 ml), which was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The concentrate was purified by means of a column chromatography (carrier: silica gel, 150 g, developing solvent: ethyl acetate-hexane, 1:1) to afford the title compound (2.56 g) as a crystalline product, m.p.117-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174877B1
Source datasetuspto-grants-2001_01
ORD IDord-79bcede3c9ec4d8babb3b4ba8296cbe6
Source noteuspto-grants-2001_01