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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178470784 | HCID 178470784 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (1-triphenylmethyl-1H-1,2,4-triazol-3-yl)acetate | HCID 54361059 | 35.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174877B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-79bcede3c9ec4d8babb3b4ba8296cbe6 |
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| Source note | uspto-grants-2001_01 |
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