تفاعل #7294
ord-40c021b30b0b44aeab08b6c10bded196
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1ترشيحthe formed precipitate of S-dibenzylcysteamine was collected by filtration
- 2استخلاصThe product was extracted with ether (3×100 mL)
- 3غسيلthe organic phase was successively washed with brine (2×100 mL)
- 4تجفيفdried over MgSO4
- 5أخرىthe solvent evaporated in vacuo
- 6أخرىIt 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.