تفاعل #1960502

ord-8b64526dadaa44299e7f2fcf7c9ca7ba

معادلة التفاعل

O=C(Cl)Cc1cccc(F)c1F
2,3-difluorophenylacetyl chloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminium(III) chloride
Cl
hydrochloric acid
C#C[Si](C)(C)C
trimethylsilylacetylene
C[Si](C)(C)c1cc2ccc(F)c(F)c2cc1O
7,8-difluoro-3-trimethylsilanylnaphthalen-2-ol

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic phase is separated off
  2. 2
    استخلاصthe aqueous phase is extracted with ethyl acetate
  3. 3
    غسيلThe combined organic phases are washed successively with sat. sodium hydrogencarbonate soln
  4. 4
    أخرىThe solution is dried
  5. 5
    أخرىevaporated to dryness
  6. 6
    أخرىThe residue is purified by column chromatography (SiO2, n-heptane:ethyl acetate=9:1)

الإجراء التجريبي

A solution of 50.0 g (0.26 mol) of 2,3-difluorophenylacetyl chloride in 100 ml of dichloromethane is slowly added to a suspension of 71.5 g (0.53 mol) of aluminium(III) chloride in 300 ml of dichloromethane at −20° C. After 30 min at this temperature, trimethylsilylacetylene is metered in, and the mixture is stirred for 30 min. The batch is added to ice-water and acidified using hydrochloric acid. The organic phase is separated off, and the aqueous phase is extracted with ethyl acetate. The combined organic phases are washed successively with sat. sodium hydrogencarbonate soln. and sat. sodium chloride soln. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:ethyl acetate=9:1), giving 7,8-difluoro-3-trimethylsilanylnaphthalen-2-ol as a brown oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08303844B2uspto-grants-2012_11