HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089856Generated: November 1, 2026
Ethyl Acetate → 2-[(2-Methoxyfluoren-9-yl)ethyl]-1,3-dioxolane
https://huagongshe.com/reaction/1089856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Methoxyfluorene | HCID 17301 | — |
| Reactant | 2-(2-Bromoethyl)-1,3-dioxolane | HCID 87776 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-[(2-Methoxyfluoren-9-yl)ethyl]-1,3-dioxolane | HCID 53866456 | 68.3% |
Reaction Steps
A solution of n-BuLi (2.5 M in hexane, 6.4 mL, 16.0 mmol) was slowly added into a cooled (-78° C.) solution of 2-methoxyfluorene (prepared according to example 10; 3.1 g, 15.8 mmol) in 100 ml THF. The reaction mixture became dark red and a solid started to precipitate out. After 30 minutes 2-(2-bromoethyl)-1,3-dioxolane (5.8 g, 32.0 mmol) was added to the cold solution and the solution was warmed up to room temperature. The reaction mixture was stirred overnight at room temperature. TLC (silica, 25% EtOAc in hexane) was used to monitor the reaction. The reaction was quenched with water and the product was extracted into EtOAc. The organic layer was washed with water (×3), dried over magnesium sulfate and evaporated. Short path chromatography (5% ethyl acetate/hexane) afforded 3.2 g (62.5%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079260 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-e88bbb653ace4aaea305f0e3d8cb53ff |
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| Source note | uspto-grants-1992_01 |
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