HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182322Generated: November 3, 2026
Water → 2-Bromo-3',4,4',5-tetrakis(2-methylbutoxy)-1,1'-biphenyl
https://huagongshe.com/reaction/1182322
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 17938208 | HCID 17938208 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-3',4,4',5-tetrakis(2-methylbutoxy)-1,1'-biphenyl | HCID 17938209 | 92% |
Reaction Steps
339 g (679.7) mmol of 3,3′,4,4′-tetra(2-methylbutyloxy)biphenyl were dissolved in 800 ml of ethyl acetate. 120.98 g (679.7 mmol) of N-bromosuccinimide were then added in solid form over a period of 15 minutes under protective gas, in the absence of light and with cooling to 0-5° C. The suspension was slowly warmed to room temperature under a blanket of protective gas and was then stirred vigorously at room temperature for 4 hours. 500 ml of ethyl acetate and 300 ml of water were added, the phases were separated and the aqueous phase was extracted twice with 100 ml each time of ethyl acetate. The combined organic phases were washed twice with 50 ml each time of water and dried over MgSO4. The oil obtained was filtered through silica gel with the aid of hexane. Taking off the solvent gave 361.2 g (625.3 mmol, 92%) of 2-bromo-4,5,3′,4′-tetra(2-methylbutyloxy)biphenyl as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288617B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-2835ee994f5546c2898283b8dad51866 |
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| Source note | uspto-grants-2007_10 |
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