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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661769Generated: October 26, 2026

Sodium Carbonate → HCID 69232322, compound

https://huagongshe.com/reaction/661769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium BicarbonateHCID 516892—
Reactant2,7-Diphenyl-9H-fluoreneHCID 15646889—
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilaneHCID 67206735—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 69232322HCID 6923232264%

Reaction Conditions

Temperature-78 °C

Reaction Steps

There was dissolved 3.00 g (9.42 mmol) of 2,7-diphenylfluorene in 60 mL of THF, and the obtained solution was cooled down to −78° C. To the solution, 6.12 mL of a 1.54 M-concentration hexane solution of n-butyllithium was added slowly, 6.12 mL of said hexane solution containing 9.42 mmol of n-butyllithium. Temperature of the resultant mixture was raised up to a room temperature, and the mixture was stirred for 2 hours at a room temperature. The mixture was cooled down to −78° C., and a solution of 3.06 g (9.42 mmol) of (2-allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilane in 14 mL of toluene was added to the mixture. Temperature of the resultant mixture was raised up to a room temperature, and the mixture was stirred for 3 hours, thereby obtaining a reaction solution. A mixture of 50 mL of a 10% aqueous solution of sodium hydrogen carbonate and 50 mL of a 10% aqueous solution of sodium carbonate was added to the reaction solution at 0° C. To the obtained mixture, 58 mL of toluene was added, and the mixture was separated to the toluene solution and the aqueous solution. The toluene solution was dried over sodium sulfate, and the mixture was filtered. The obtained filtrate was concentrated under a reduced pressure. A small amount of toluene was added the concentrated filtrate to obtain a solution, and hexane was further added thereto, thereby obtaining 3.66 g (yield: 64.0%) of (2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-diphenyl fluoren-9-yl)diethylsilane as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084559B2
Source datasetuspto-grants-2011_12
ORD IDord-30812e22092e4a339b70367b310379d2
Source noteuspto-grants-2011_12