HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639686Generated: October 31, 2026
1-Azido-4-methoxybenzene → 5-(2,4-Dichlorophenyl)-3-(4-methoxyphenyl)triazol-4-amine
https://huagongshe.com/reaction/1639686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Azido-4-methoxybenzene | HCID 75004 | — |
| Reactant | 2,4-Dichlorophenylacetonitrile | HCID 80566 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(2,4-Dichlorophenyl)-3-(4-methoxyphenyl)triazol-4-amine | HCID 25215443 | 25.4% |
Reaction Steps
To an ice-cooled and stirred mixture of 1-azido-4-methoxy-benzene (0.750 g, 1 eq) and commercial (2,4-dichloro-phenyl)-acetonitrile (1.12 g, 1.2 eq) in ethanol (10 ml) kept under nitrogen, a solution of sodium methoxide (0.408 g, 1.5 eq) in ethanol (10 ml) is added drop-wise (25 min). After the addition, the reaction mixture is allowed to reach room temperature spontaneously and stirring is then continued overnight at room temperature. The resulting reaction mixture is diluted with ethyl acetate (40 ml), washed with water (2×50 ml), dried over MgSO4 and evaporated to dryness. The yellow semisolid residue (0.842 g) is purified by flash chromatography using 60-120 mesh silica gel and eluting with 15% ethylacetate in hexane, to afford the title compound as a white solid (0.428 g, 24% yield). M.p. 154.6-163.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110588B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-67709d0011cb4a1bbcc068801243af2c |
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| Source note | uspto-grants-2012_02 |
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