تفاعل #966
ord-ecbc4c566e744d9b960cfaf350b242df
معادلة التفاعل
3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine
→
title compound
المردود 67.1%
3-(N-tert-butyloxycarbonylaminomethyl) azetidine
المردود 67.1%
الكواشف
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1ترشيحThe catalyst was filtered off
- 2أخرىthe solvent evaporated
- 3أخرىThe crude product was purified by flash chromatography
الإجراء التجريبي
3.4 g (9.6 mmol) of 3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine was dissolved in 170 mL MeOH and hydrogenated over 0.30 g Pd(OH)2 at 5 MPa over night. The catalyst was filtered off and the solvent evaporated. The crude product was purified by flash chromatography using MeOH/CH2Cl2, 1/9, followed by MeOH (saturated with NH3 (g))/CH2Cl2, 1/9, as eluent to yield 1.2 g (67%) of the title compound.