تفاعل #69566

ord-5cb30b4366f44281b496e7a76d17fed4

معادلة التفاعل

Cc1ccccc1-c1ccccc1C
2,2′-dimethylbiphenyl
BrC12CC3CC(CC(C3)C1)C2
1-bromo-adamantane
Cc1ccc(C23CC4CC(CC(C4)C2)C3)cc1-c1cc(C23CC4CC(CC(C4)C2)C3)ccc1C
2,2′-dimethyl-5,5′-bis(1-adamantyl)biphenyl
المردود 48.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 100 ml four-neck flask provided with a thermometer, stirrer
  2. 2
    درجة الحرارةreflux tube
  3. 3
    workup.ADDITIONnitrogen-introducing tube
  4. 4
    workup.STIRRINGthe result stirred at room temperature
  5. 5
    workup.DISSOLUTIONuntil dissolving
  6. 6
    درجة الحرارةAn oil bath was heated to 60° C.
  7. 7
    ترشيحThe reaction solution was filtered
  8. 8
    غسيلrinsed away with a small amount of methanol
  9. 9
    workup.STIRRINGThe filtered material was stirred in 30 ml of methanol for 30 minutes
  10. 10
    ترشيحfiltered
  11. 11
    أخرىThe obtained residue was dried at 60° C. under reduced pressure

الإجراء التجريبي

A 100 ml four-neck flask provided with a thermometer, stirrer, reflux tube, and nitrogen-introducing tube was charged with 2,2′-dimethylbiphenyl 14.7 g (80.55 mmol), 1-bromo-adamantane 34.7 g (161.1 mmol), and nitromethane 200 ml and the mixture stirred under a nitrogen flow at room temperature. Iron (III) chloride 1.31 g (8.07 mmol) was added and the result stirred at room temperature until dissolving. An oil bath was heated to 60° C., then the stirring was continued at that temperature for 4 hours. The reaction solution was filtered and rinsed away with a small amount of methanol. The filtered material was stirred in 30 ml of methanol for 30 minutes, then filtered. The obtained residue was dried at 60° C. under reduced pressure to obtain 2,2′-dimethyl-5,5′-bis(1-adamantyl)biphenyl white powder 17.5 g.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530596B2uspto-grants-2013_09