Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | 2-(1-Chloroethyl)-9H-fluorene | HCID 14572484 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22372689 | HCID 22372689 | — |
Reaction Steps
The thus obtained 2-(1-chloroethyl)-9H-fluorene was mixed with 1,2,4-triazole (1.31 g) and heated at 120° C. for 30 minutes without further adding solvent. After cooling, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated and then the resulting residue was subjected to silica gel column chromatography. First, elution was carried out with a mixed solvent of chloroform and methanol (50:1), and the thus obtained crude crystals were recrystallized from a mixed solvent of ether and ethyl acetate to obtain 0.24 g of 1-[1-(9H-fluoren-2-yl) ethyl]-1H-1,2,4-triazole (Example 5). Thereafter, crude crystals obtained from the chloroform-methanol (50:1) eluate were recrystallized from a mixed solvent of ethyl acetate and ether to obtain 0.25 g of 4-[1-(9H-fluoren-2-yl) ethyl]-4H-1,2,4-triazole (Example 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807880 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-53072c8fe8e541ee852c40d180f35759 |
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| Source note | uspto-grants-1998_09 |
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