تفاعل #488899

ord-86ae72377164440ba05b146cd08679de

معادلة التفاعل

COC(=O)c1ccc(C2(c3ccccc3)SCCS2)cc1
64b
COC(=O)c1ccc(C2(c3ccccc3)SCCS2)cc1
Methyl 4-(2-phenyl-1,3-dithiolan-2-yl)benzoate
F[B-](F)(F)F.F[B-](F)(F)F.F[N+]12CC[N+](CCl)(CC1)CC2
Selectfluor
F.c1ccncc1
HF-pyridine
COC(=O)c1ccc(C(F)(F)c2ccccc2)cc1
compound 64c
COC(=O)c1ccc(C(F)(F)c2ccccc2)cc1
Methyl 4-(difluoro(phenyl)methyl)benzoate

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىthe consumption of all 64b
  2. 2
    workup.ADDITIONthe reaction was diluted with CH2Cl2
  3. 3
    تجفيفThe combined organics were dried over anhydrous Na2SO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe crude product was purified by flash column chromatography (silica gel, 5% EtOAc/hexanes)

الإجراء التجريبي

Selectfluor (1.07 mmol, 381 mg) and HF-pyridine reagent (1.5 mL, HF: Pyridine=70:30 wt %) were dissolved in CH2Cl2 (4 mL) in a polyethylene bottle and cooled to 0° C. A solution of 64b (0.512 mmol, 162 mg) in CH2Cl2 (2 mL) was slowly added and the mixture was stirred for 45 min at room temperature. When TLC indicated the consumption of all 64b, the reaction was diluted with CH2Cl2. The combined organics were dried over anhydrous Na2SO4 and concentrated. The crude product was purified by flash column chromatography (silica gel, 5% EtOAc/hexanes) to afford compound 64c as a clear oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741887B2uspto-grants-2014_06