HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221174Generated: October 25, 2026
Tetrahydrofuran → 9,9-dibutyl-2-iodo-9H-fluorene
https://huagongshe.com/reaction/221174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | 2-Iodo-9H-fluorene | HCID 224094 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 9,9-dibutyl-2-iodo-9H-fluorene | HCID 23072853 | — |
Reaction Steps
Under N2 atmosphere, 0.58 parts of 2-iodo-9H-fluorene, 1.10 parts of 1-iodobutane, and 0.67 parts of potassium tert-butoxide were added into 15 parts of dry tetrahydrofuran, followed by stirring and mixing. Then, the reaction mixture was heated to 50° C. and reacted for 12 hours. After the reaction mixture was cooled, poured the water into the reaction mixture for quenching the reaction, using the diethyl ether to extract the product, and magnesium sulfate was used for dehydration. After removing the solvent, the residual was purified with column chromatography method by using hexane as an eluent, to obtain a compound (32) of the present example. This compound was in a form of a light yellow solid, and the yield of this compound was 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08203068B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-67fe20fafb014f069195b70da1c871fe |
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| Source note | uspto-grants-2012_06 |
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