تفاعل #7294

ord-40c021b30b0b44aeab08b6c10bded196

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe formed precipitate of S-dibenzylcysteamine was collected by filtration
  2. 2
    استخلاصThe product was extracted with ether (3×100 mL)
  3. 3
    غسيلthe organic phase was successively washed with brine (2×100 mL)
  4. 4
    تجفيفdried over MgSO4
  5. 5
    أخرىthe solvent evaporated in vacuo
  6. 6
    أخرىIt could, however be recrystallized from ethyl acetate

الإجراء التجريبي

To a suspension of 0.1 mole cysteamine hydrochloride in 20 mL methanol were added 13.6 mL of 25% ammonia solution, followed by dropwise addition of 0.12 mole benzyl bromide at room temperature. The mixture was stirred for 0.5 h, and the formed precipitate of S-dibenzylcysteamine was collected by filtration. The product was extracted with ether (3×100 mL) and the organic phase was successively washed with brine (2×100 mL), dried over MgSO4 and the solvent evaporated in vacuo. The crude product was essentially pure enough for the next step. It could, however be recrystallized from ethyl acetate. Yield 86%, of white solid. m.p. 85–6° C. NMR (CDCl3) in agreement with the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084244B2uspto-grants-2006_08