تفاعل #2507816
ord-3368c914e50e4d339da174b0786643cd
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المعالجة
- 1درجة الحرارةThe solution was cooled to below −10° C. by ice/acetone bath
- 2أخرى10° C.
- 3workup.STIRRINGsolution was stirred for an additional two hours after which GC-MS
- 4أخرىhad reacted
- 5غسيلit was washed twice with 500 ml water
- 6أخرىThe organic layer was collected
- 7أخرىpentane was evaporated
- 8workup.DISSOLUTIONRemaining material was dissolved to 700 ml ethanol
- 9workup.ADDITIONa small amount of water was added
- 10درجة الحرارةThe solution was then heated up
- 11درجة الحرارةto reflux
- 12workup.STIRRINGit was stirred for 15 h
- 13درجة الحرارةAfter cooling down to room temperature the solution
- 14ترشيحwas filtered
- 15workup.ADDITION300 ml water was added
- 16استخلاصthe product was extracted
- 17غسيلby washing twice with 500 ml pentane
- 18أخرىPentane layers were collected
- 19غسيلwashed once with water
- 20أخرىThe organic layer were collected
- 21تجفيفdried with anhydrous magnesium sulfate
- 22ترشيحfiltered
- 23أخرىPentane was evaporated
- 24workup.DISTILLATIONwas purified by distillation, yield 45.90 g (67%)
- 25أخرى1-allyl-3,5-dimethyladamantane was moved to a 100 ml vessel
- 26درجة الحرارةThe solution was heated up to 85° C.
- 27workup.ADDITIONAfter addition
- 28درجة الحرارةthe solution was heated up to 100° C.
- 29workup.STIRRINGit was stirred for an hour
- 30أخرىThe product thus obtained
- 31workup.DISTILLATIONwas then purified by distillation
- 32أخرىyielding 53.54 g (51%), bp. 157-158° C./<0.5 mbar
الإجراء التجريبي
81.71 g (0.336 mol) 3,5-dimethyladamantylbromide was dissolved in 500 ml pentane. The solution was cooled to below −10° C. by ice/acetone bath. 51.40 g (0.425 mol) allylbromide was added followed by 410 mg FeBr3. The solution was then stirred for three hours at −20 . . . 10° C. after which analysis by GC-MS was carried out, indicating that some unreacted starting materials remained. 420 mg FeBr3 was added and solution was stirred for an additional two hours after which GC-MS showed that all the dimethyladamantyl bromide had reacted. The solution was warmed up to room temperature and it was washed twice with 500 ml water. The organic layer was collected and pentane was evaporated. Remaining material was dissolved to 700 ml ethanol and a small amount of water was added followed by 25 g (0.382 mol) metallic zinc. The solution was then heated up to reflux and it was stirred for 15 h. After cooling down to room temperature the solution was filtered. 300 ml water was added and the product was extracted by washing twice with 500 ml pentane. Pentane layers were collected and washed once with water. The organic layer were collected, dried with anhydrous magnesium sulfate and filtered. Pentane was evaporated and remaining crude 1-allyl-3,5-dimethyladamantane was purified by distillation, yield 45.90 g (67%). 1-allyl-3,5-dimethyladamantane was moved to a 100 ml vessel followed by 50 μl H2PtCl6/IPA solution. The solution was heated up to 85° C. and 59.50 g (0.227 mol) 1,1,1,4,4-pentachloro-1,4-disilabutane was added slowly during 30 min. After addition, the solution was heated up to 100° C. and it was stirred for an hour. The product thus obtained was then purified by distillation yielding 53.54 g (51%), bp. 157-158° C./<0.5 mbar.