تفاعل #9377

ord-39187aa04b4741c7af65c404933627df

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    تركيزAs the mixture was concentrated
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in CH2Cl2
  3. 3
    أخرىAfter 1 h the mixture was quenched with water
  4. 4
    أخرىthe layers were separated
  5. 5
    استخلاصThe aqueous layer was extracted with Et2O (3×150 mL)
  6. 6
    غسيلthe combined organic extracts were washed with H2O (3×100 mL), saturated NaHCO3 (3×100 mL), brine (1×100 mL)
  7. 7
    تجفيفdried over MgSO4
  8. 8
    تركيزconcentrated

الإجراء التجريبي

4-Bromo-indan-1-one was obtained by the following procedure: A solution of 3-(2-bromo-phenyl)-propionic acid (commercially available from Oakwood Products) (15.0 g, 65.5 mmol) in CH2Cl2 at 0° C. was reacted with oxalyl chloride (7.2 mL, 1.5 eq) followed by 2–3 drops of DMF. The mixture was stirred until no more gas evolution was observed. As the mixture was concentrated and the residue was dissolved in CH2Cl2, cooled to 0° C., and treated with AlCl3 (9.6 g, 1.1 eq). After 1 h the mixture was quenched with water and the layers were separated. The aqueous layer was extracted with Et2O (3×150 mL) and the combined organic extracts were washed with H2O (3×100 mL), saturated NaHCO3 (3×100 mL), brine (1×100 mL), dried over MgSO4 and concentrated. 4-Bromoindan-1-one, 10.5 g (76%) was obtained by chromatography using 10% EtOAc:hexane as eluant. Use of 4-bromo-indan-1-one in Method NINETEEN produced 4-(4-bromo-indan-2-yl)-1,3-dihydro-imidazole-2-thione (Compound 149).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091232B2uspto-grants-2006_08