تفاعل #1487

ord-d9c61c395e2c4475a549c72777a848f0

معادلة التفاعل

COC(=O)c1ccc2c(c1)C(OS(=O)(=O)C(F)(F)F)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(trifluoromethylsulfonyl)oxy-naphthalene-2-carboxylate
COC(=O)c1ccc2c(c1)C(OS(=O)(=O)C(F)(F)F)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(trifluoromethylsulfonyl)oxy-naphthalene -2-carboxylate
COC(=O)c1ccc2c(c1)C(OS(=O)(=O)C(F)(F)F)=CCC2(C)C
Compound E4
COC(=O)c1ccc2c(c1)C(OS(=O)(=O)C(F)(F)F)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(trifluoromethylsulfonyl)oxy-naphthalene -2-carboxylate
c1ccsc1
thiophene
[Li][CH2]CCC
n-butyllithium
COC(=O)c1ccc2c(c1)C(c1cccs1)=CCC2(C)C
title compound
COC(=O)c1ccc2c(c1)C(c1cccs1)=CCC2(C)C
Methyl 5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalene-2-carboxylate

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe resulting solution stirred for 30 minutes
  2. 2
    workup.ADDITIONThis solution was added to a second flask
  3. 3
    درجة الحرارةthe resulting solution was heated to 50° C. for 3 h
  4. 4
    درجة الحرارةUpon cooling to room temperature the reaction
  5. 5
    أخرىwas quenched by the addition of saturated aqueous NH4Cl
  6. 6
    استخلاصExtraction with EtOAc
  7. 7
    غسيلby washing of the combined organic layers with H2O and saturated aqueous NaCl
  8. 8
    تجفيفdrying over MgSO4
  9. 9
    تركيزThe dry solution was concentrated under reduced pressure

الإجراء التجريبي

(Compound E5) To a solution of 329.0 mg (3.93 mmol) of thiophene in 2.0 mL THF at 0° C. was added 251.8 mg (3.93 mmol, 1.56 mL of 2.5M solution in hexanes) of n-butyllithium. After stirring for 3 h at 0° C., a solution of 845.0 mg (6.28 mmol) of ZnCl2 in 5.0 mL THF was added and the resulting solution stirred for 30 minutes. This solution was added to a second flask containing 570.0 mg (1.57 mmol) of methyl 5,5-dimethyl-5,6-dihydro-8-(trifluoromethylsulfonyl)oxy-naphthalene-2-carboxylate (Compound E4) and 76.0 mg (0.063 mmol) of tetrakis(triphenyphosphine)palladium(0) in 4.0 mL THF, and the resulting solution was heated to 50° C. for 3 h. Upon cooling to room temperature the reaction was quenched by the addition of saturated aqueous NH4Cl. Extraction with EtOAc was followed by washing of the combined organic layers with H2O and saturated aqueous NaCl, and drying over MgSO4. The dry solution was concentrated under reduced pressure and the title compound was isolated from the residue as a yellow oil by column chromatography (5-10% EtOAc/hexanes).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723666uspto-grants-1998_03