تفاعل #586125

ord-dbdc957797184312a7eb0f8e9262850a

معادلة التفاعل

CCOCOc1ccc(-c2ccc(C(F)(F)F)cc2)cc1Sc1cc(-c2ccc(C(F)(F)F)cc2)ccc1OCOCC
1,1′-thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene]
O=S([O-])CO.[Na+]
Rongalite
O=C([O-])[O-].[K+].[K+]
potassium carbonate
FC(F)(F)CI
2,2,2-trifluoroethyl iodide
CCOCOc1ccc(-c2ccc(C(F)(F)F)cc2)cc1SCC(F)(F)F
[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide
المردود 151.1%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting reaction mixture
  2. 2
    استخلاصextracted with 50 ml of ethyl acetate twice
  3. 3
    غسيلThe ethyl acetate layer was washed with 50 ml of water twice
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
  6. 6
    أخرىPurification of the residue by silica gel column chromatography

الإجراء التجريبي

3.3 g (5.0 mmol) of 1,1′-thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene], 3.0 g (19.5 mmol) of Rongalite, 3.0 g (21.7 mmol) of potassium carbonate and 3.2 g (17.6 mmol) of 2,2,2-trifluoroethyl iodide were stirred in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 3.1 g of [2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide (yield 75.6%) as a pale yellow viscous liquid (nD20 1.5213).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767626B2uspto-grants-2010_08