تفاعل #50901

ord-8ba09fd2cc7646759768ea7fc99b2cf3

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added to a round bottom flask
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    workup.ADDITIONcontaining the resulting mixture
  3. 3
    workup.ADDITIONwere added drop-wise
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    أخرىThen, the mixture was reacted for 2 hours
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    درجة الحرارةthe resulting mixture was refluxed for 12 hours
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    استخلاصThen, the organic layer was extracted from the reaction solution
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    تجفيفdried with anhydrous sodium sulfate
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    أخرىNext, after evaporating the solvent
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    أخرىto obtain an oily residue
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    أخرىa rotary evaporator
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    أخرىthe product was separated

الإجراء التجريبي

(Step-2) Magnesium metal(2.6 g) and anhydrous tetrahydrofuran (hereinafter referred to as THF(100 mL)) were added to a round bottom flask. Next, after dripping a small quantity of dibromoethane into the round bottom flask containing the resulting mixture to promote the reaction, 3-chloropropyl vinyl ether (12 g, 0.1 mol) and anhydrous THF(100 mL) were added drop-wise thereto. Then, the mixture was reacted for 2 hours. After dripping an adequate quantity of THF containing 2-adamantanone (15 g, 0.1 mol) in the mixture, the resulting mixture was refluxed for 12 hours. After the reaction was completed, the reaction mixture was slowly dissolved in excessive water and neutralized with thin H2SO4 solution. Then, the organic layer was extracted from the reaction solution using an adequate quantity of diethyl ether and then dried with anhydrous sodium sulfate. Next, after evaporating the solvent to obtain an oily residue using a rotary evaporator, the product was separated using a column chromatography method (hexane:ethyl acetate=3:1). (Yield: 60%)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849378B2uspto-grants-2005_02