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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,7-Bis(phenyl-m-tolylamino)-9,9-bis[2-(methoxycarbonyl)ethyl]fluoreneHCID 14597879—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2,7-Bis(phenyl-m-tolylamino)-9,9-bis(3-hydroxypropyl)fluoreneHCID 1459788096.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853308
Source datasetuspto-grants-1989_08
ORD IDord-133c1a59fe694d91b08e83dac7ea8595
Source noteuspto-grants-1989_08