تفاعل #54455

ord-35cc3eed3fdd4c9c830572cf9db82737

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةto reflux for 30 minutes
  3. 3
    درجة الحرارةthe mixture refluxed 30 minutes
  4. 4
    درجة الحرارةthe mixture refluxed for 15 minutes
  5. 5
    غسيلThe organic phase was washed with brine
  6. 6
    أخرىdried
  7. 7
    تركيزconcentrated

الإجراء التجريبي

A solution of ethyl bromide (1.75 g.) in diethyl ether was added to a suspension of magnesium (0.385 g.) in ether and the mixture was heated to reflux for 30 minutes. A solution of the alcohol, 3-hydroxy-3,7-dimethyl-nona-4,6,8-trien-1-yne, (1.0 g.) in dry benzene was added and the mixture refluxed 30 minutes. A solution of 2,2,6-trimethylcyclohexanone (1.12 g.) in benzene was added and the mixture refluxed for 15 minutes and poured into saturated aqueous ammonium chloride solution. The organic phase was washed with brine dried and concentrated to give 7-hydroxy-3,7-dimethyl-9-(1-hydroxy-2,2,6-trimethylcyclohexyl)-nona-1,3,5-trien-8-yne which was chromatographed on activity III alumina to give pure 7-hydroxy-3,7-dimethyl-9-(1-hydroxy-2,2,6-trimethyl-cyclohexyl)-nona-1,3,5-trien-8-yne.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04148829uspto-grants-1979_04