تفاعل #65653

ord-59a33a6faa3c4cb4bbf81a1b1cabcf6a

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحFilter
  2. 2
    أخرىevaporate the solvent in vacuo
  3. 3
    أخرىPartition between water (125 mL) and ether (75 mL)
  4. 4
    أخرىSeparate the aqueous phase
  5. 5
    استخلاصExtract with methylene chloride (75 mL)
  6. 6
    تجفيفdry (Na2SO4)
  7. 7
    أخرىevaporate the solvent in vacuo
  8. 8
    أخرىPurify by silica gel chromatography (2:1 hexane/ethyl acetate)

الإجراء التجريبي

Dissolve 2-(carbomethoxy)-2-(4-methoxybenzylthio)indan (2.20 g, 3.55 mmol) in 95% ethanol (25 mL), water (12 mL) and tetrahydrofuran (15 mL). Treat with potassium hydroxide (1.3 g, 2 3 mmol) and stir at room temperature for 1 hour. Filter and evaporate the solvent in vacuo. Partition between water (125 mL) and ether (75 mL). Separate the aqueous phase and acidify with cold concentrated hydrochloric acid. Extract with methylene chloride (75 mL), dry (Na2SO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (2:1 hexane/ethyl acetate) to give 2-carboxy-2-(4-methoxybenzylthio)indan as a yellow solid (0.48 g, 43%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420271uspto-grants-1995_05