تفاعل #792139

ord-4b645423b9854dc9b8ccb262ffda2245

معادلة التفاعل

[H-].[Na+]
sodium hydride
C[S+](C)C.[I-]
trimethylsulfonium iodide
CCC(=O)c1ccc(Oc2ccc(Cl)cc2)cc1Cl
1-[2-chloro-4-(4-chlorophenoxy)phenyl]propan-1-one
CCC1(c2ccc(Oc3ccc(Cl)cc3)cc2Cl)CO1
2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-ethyl-oxirane
المردود 107.5%

المذيبات

ظروف التفاعل

درجة الحرارة
5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe resulting mixture was then warmed to room temperature overnight
  2. 2
    أخرىquenched with an aqueous solution of ammonium chloride and iced water
  3. 3
    استخلاصextracted with MTBE
  4. 4
    غسيلThe organic solvents were washed with water
  5. 5
    أخرىdried
  6. 6
    أخرىevaporated

الإجراء التجريبي

To a solution of sodium hydride (35.72 g, 1.49 mol) in THF (1 L) and dry DMSO (2 L) was added under argon drop wise at 5° C. a solution of trimethylsulfonium iodide (290.5 g, 1.42 mol) in dry DMSO (2 L). The mixture was stirred 1 hour at 5° C. followed by a dropwise addition of 1-[2-chloro-4-(4-chlorophenoxy)phenyl]propan-1-one (199.0 g, 0.65 mol) in DMSO (500 mL). The resulting mixture was then warmed to room temperature overnight and quenched with an aqueous solution of ammonium chloride and iced water, and then extracted with MTBE. The organic solvents were washed with water, dried and evaporated to give 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-ethyl-oxirane as a yellowish solid (216.0 g, 97%). 1H-NMR (CDCl3; 400 MHz) • • (ppm)=0.9 (t, 3H); 1.75 (m, 1H); 2.10 (m, 1H); 2.80 (d, 1H); 3.05 (d, 1H); 6.85 (d, 1H); 6.95 (m, 3H); 7.30 (d, 2H); 7.40 (d, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09173402B2uspto-grants-2015_11