HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661769Generated: October 26, 2026
Sodium Carbonate → HCID 69232322, compound
https://huagongshe.com/reaction/661769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,7-Diphenyl-9H-fluorene | HCID 15646889 | — |
| Reactant | (2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilane | HCID 67206735 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 69232322 | HCID 69232322 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084559B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-30812e22092e4a339b70367b310379d2 |
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| Source note | uspto-grants-2011_12 |
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