Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Fluorene | HCID 6853 | — |
| Reactant | Hexane | HCID 8058 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Fluorene-9-ethanol | HCID 10921761 | — |
Reaction Steps
2-(9-Fluorenyl) ethanol was prepared from a solution of fluorene (116.35 g, 0.7 mmol) in 800 ml of dry THF at -20° C. which was added n-Buli in hexane (0.7 mol) keeping the temperature below -10° C. To the clear solution was rapidly added 357 ml of 1.4M ethylene oxide in ether (0.5 mol) keeping the temperature below 5° C. The reaction mixture was stirred for 5 hours, then quenched with 50 ml of saturated ammonium chloride solution. The THF was removed at a rotary evaporator. The residue was partitioned between water and ethyl acetate. The organic layer was separated, dried with MgSO4 and concentrated in vacuo until crystallization began. The solution was allowed to stand overnight and the crystals were collected and dried (mp 97° C.) (85.5 g, (81%)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05519043 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-03bf240bba5a4506a74b496c68aa80a8 |
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| Source note | uspto-grants-1996_05 |
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