HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721838Generated: November 1, 2026
Sodium Hydroxide → 2,7-Bis(phenyl-m-tolylamino)-9,9-bis(3-hydroxypropyl)fluorene
https://huagongshe.com/reaction/1721838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,7-Bis(phenyl-m-tolylamino)-9,9-bis[2-(methoxycarbonyl)ethyl]fluorene | HCID 14597879 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,7-Bis(phenyl-m-tolylamino)-9,9-bis(3-hydroxypropyl)fluorene | HCID 14597880 | 96.3% |
Reaction Steps
To a well-stirred solution of 8.8 grams of 9,9-bis[2-(methoxycarbonyl)ethyl]-2,7-bis(phenyl-m-tolylamino)fluorene in 150 milliliters of dried tetrahydrofuran under a nitrogen atmosphere was added in small portions, 0.52 gram, of lithium aluminum hydride over a period of 15 to 30 minutes. The reaction mixture was stirred at room temperature for two hous. Ten percent aqueous sodium hydroxide solution was then slowly added to the reaction mixture. The organic layer was separated and evaporated to dryness under reduced pressure. The residue as dissolved in methylene chloride, and washed several times with water. Evaporation of the dry methylene chloride solution provided a white solid, which was recrystallized from isopropanol and water to yield 7.8 grams of the above fluorene pure product, melting point, 216° to 217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853308 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-133c1a59fe694d91b08e83dac7ea8595 |
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| Source note | uspto-grants-1989_08 |
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