تفاعل #1687649

ord-0ef7506cc8324ddcb4daf9be46433a35

معادلة التفاعل

CC[C@H]1CC[C@H]([C@H]2CC[C@H](C=O)CC2)CC1
trans-4-(trans-4-ethylcyclohexyl)cyclohexane carboaldehyde
FC(Br)(Br)Br
tribromofluoromethane
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenyl phosphine
CC[C@H]1CC[C@H]([C@H]2CC[C@H](C=C(F)Br)CC2)CC1
trans-4-(trans-4-ethylcyclohexyl)cyclohexyl-2-fluoro-2-bromoethene

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction solution was cooled with ice
  2. 2
    أخرىwere removed by filtration
  3. 3
    workup.ADDITIONDilute hydrochloric acid was added to the filtrate, and it
  4. 4
    استخلاصwas extracted with toluene
  5. 5
    غسيلAfter the organic layer was washed with water, it
  6. 6
    أخرىwas dried
  7. 7
    تركيزconcentrated under a reduced pressure
  8. 8
    أخرىto obtain a brown oily product
  9. 9
    أخرىAfter this product was purified
  10. 10
    أخرىwas recrystallized from heptane

الإجراء التجريبي

A solution of tribromofluoromethane and triphenyl phosphine in ethylene glycol dimethyl ether was stirred at 70° C. for 1 hour. The reaction solution was cooled with ice, and a solution of trans-4-(trans-4-ethylcyclohexyl)cyclohexane carboaldehyde in tetrahydrofuran was added thereto. After the reaction solution was further stirred for 1 hour, the temperature of the solution was gradually raised up to room temperature, and insoluble substances were removed by filtration. Dilute hydrochloric acid was added to the filtrate, and it was extracted with toluene. After the organic layer was washed with water, it was dried by using anhydrous magnesium sulfate, and concentrated under a reduced pressure to obtain a brown oily product. After this product was purified by using a silica gel column chromatography, it was recrystallized from heptane to obtain trans-4-(trans-4-ethylcyclohexyl)cyclohexyl-2-fluoro-2-bromoethene.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05976408uspto-grants-1999_11