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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661764Generated: October 25, 2026

Sodium Carbonate → HCID 69232287, compound

https://huagongshe.com/reaction/661764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium hydrideHCID 82127—
ReactantSodium BicarbonateHCID 516892—
Reactant2,7-Di-tert-butylfluoreneHCID 4090082—
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilaneHCID 67206735—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 69232287HCID 69232287—

Reaction Steps

There was washed 3.00 g (22.45 mmol) of potassium hydride having a purity of 30% by weight with each 6 mL of hexane three times in an atmosphere of nitrogen, and 37 mL of THF was added thereto. To the obtained THF slurry of potassium hydride, 5.00 g (17.96 mml) of 2,7-di-tert-butylfluorene was added dropwise at 0° C. using 32 mL of a THF solution thereof. The obtained mixture was stirred for 2.5 hours at a room temperature, and then 5.84 g (17.96 mmol) of (2-allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilane was added dropwise at −78° C. using 7 mL of a toluene solution thereof. The temperature of the obtained liquid reaction mixture was raised up to a room temperature, and the mixture was stirred for 2.5 hours. The mixture was added dropwise at 0° C. to a mixture of 32 mL of a 10% aqueous solution of sodium hydrogen carbonate and 32 mL of a 10% aqueous solution of sodium carbonate, and the resultant mixture was extracted with 20 mL of toluene. The obtained extract was dried over sodium sulfate, and the solvent contained therein was distilled away under a reduced pressure, thereby obtaining quantitatively (2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butyl fluoren-9-yl)diethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084559B2
Source datasetuspto-grants-2011_12
ORD IDord-a90075989d514cb2827234811c32f0f7
Source noteuspto-grants-2011_12