HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628369Generated: November 2, 2026
Tetrahydrofuran → 2,4-Bis-(4-tert-butylphenyl)-6-(4'-vinylbiphenyl-4-yl)-1,3,5-triazine
https://huagongshe.com/reaction/1628369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(4-Bromophenyl)-4,6-bis(4-tert-butylphenyl)-1,3,5-triazine | HCID 59439787 | — |
| Reactant | Ethenoxy(phenyl)borinic acid | HCID 66674744 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 2,4-Bis-(4-tert-butylphenyl)-6-(4'-vinylbiphenyl-4-yl)-1,3,5-triazine | HCID 59439782 | — |
Reaction Steps
2.0 g (0.0040 mol) of 2-(4-bromophenyl)-4,6-bis-(4-tert-butylphenyl)-1,3,5-triazine and 0.8878 g (0.006 mol) of vinylphenylboronic acid and 0.050 g (0.0432 mmol) of Pd(PPh3)4 are initially introduced. After addition of 26 ml of sodium carbonate solution and 54 ml of THF, the mixture is brought to reaction under reflux for 24 h. For work-up, the mixture is filtered through Celite and taken up in ethyl acetate. The organic phase is extracted a number of times with water. The solvent of the combined organic phases is removed completely. A recrystallisation is carried out from chloroform/ethanol, and subsequent column chromatography is carried out with hexane:ethyl acetate. After the column chromatography, 1.6 g (76%) of clean substance are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08786181B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-639465824ba44125be47b249a50c6c3c |
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| Source note | uspto-grants-2014_07 |
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