تفاعل #490488

ord-2fcad731f42c4bcc820b327965c9d861

معادلة التفاعل

COC(=O)c1ccc(C2(c3ccccc3)SCCS2)cc1
compound 18b
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
1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
F.c1ccncc1
HF-pyridine
COC(=O)c1ccc(C(F)(F)c2ccccc2)cc1
compound 18c
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
    استخلاصThe solution was extracted with CH2Cl2
  2. 2
    تجفيفthe combined organics were dried over anhydrous Na2SO4
  3. 3
    تركيزconcentrated
  4. 4
    أخرىA crude product was purified by flash column chromatography (silica gel, 5% EtOAc/hexanes)

الإجراء التجريبي

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) (381 mg, 1.07 mmol) 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 compound 18b (162 mg, 0.512 mmol) in CH2Cl2 (2 mL) was slowly added and the mixture was stirred for 45 min at room temperature. The solution was extracted with CH2Cl2, and the combined organics were dried over anhydrous Na2SO4 and concentrated. A crude product was purified by flash column chromatography (silica gel, 5% EtOAc/hexanes) to afford compound 18c as a clear oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08748417B2uspto-grants-2014_06