HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41287Generated: October 25, 2026
1,3-Dibromobenzene → 3,3',5,5'-Tetramethyl-7,7'-bis(3,5-dibromophenyl)-1,1'-biadamantane
https://huagongshe.com/reaction/41287
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Bromhydrol | HCID 166749 | — |
| Reactant | 3,3'-Dibromo-5,5',7,7'-tetramethyl-1,1'-biadamantane | HCID 57934707 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3,3',5,5'-Tetramethyl-7,7'-bis(3,5-dibromophenyl)-1,1'-biadamantane | HCID 57558380 | 180% |
Reaction Steps
A 3-liter recovery flask was charged with the above synthesized 7,7′-dibromo-3,3′,5,5′-tetramethyl-1,1′-biadamantane 48.4 g (100 mmol), 1,3-dibromo benzene 1180 g (500 mmol), and a stirrer. While stirring under a nitrogen flow at room temperature, aluminum bromide (III) 26.7 g (100 mmol) was added little by little. After the end of addition, the solution was stirred at 50° C. for 7 hours. The reaction solution was charged into a 1 mol/liter hydrochloric acid solution 2 liter, the aqueous phase was removed by separation, then acetone 1 liter was added for extraction. The solid was collected by filtration and dried under reduced pressure to obtain 7,7′-bis(3,5-dibromophenyl)-3,3′,5,5′-tetramethyl-1,1′-biadamantane (90.0 mmol; yield 90.0%) 71.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530596B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-482d535ef50f4cb0ae074e5269c7e9b0 |
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| Source note | uspto-grants-2013_09 |
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