HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166416Generated: October 27, 2026
1H-1,2,4-Triazole → 1-(1H-1,2,4-triazol-1-yl)-2-isopropoxy-2-(2,4-dichlorophenyl)pentane
https://huagongshe.com/reaction/2166416
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Azodicarboxylic acid dimethyl ester | HCID 351621 | — |
| Reactant | 2-(2,4-Dichlorophenyl)-2-isopropoxypentan-1-ol | HCID 23039713 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1H-1,2,4-triazol-1-yl)-2-isopropoxy-2-(2,4-dichlorophenyl)pentane | HCID 23039686 | — |
Reaction Steps
A solution of 5.5 g (30 mmoles) of dimethyl azodicarboxylate is added dropwise, at room temperature, to a solution of 5.8 g (20 mmoles) of 2-(2,4-dichlorophenyl)-2-isopropoxypentan-1-ol, 7.9 g (30 mmoles) of triphenylphosphine and 1.66 g (24 mmoles) of 1,2,4-triazole in 100 ml of absolute tetrahydrofuran, and the reaction mixture is then stirred for 3 hours at room temperature and then for a further 16 hours at 50° C. and is evaporated; the residue is digested with 100 ml of diethyl ether, the insoluble residue is filtered off, and the ether phase is concentrated again and purified by column chromatography (silica gel; 1:1 ethyl acetate/petroleum ether). This gives a colourless oil having physical data which agree entirely with those in Example 3b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04945100 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-a1dba695f8394a7299a3bd7fff9ac90f |
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| Source note | uspto-grants-1990_07 |
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