تفاعل #1884982
ord-e9bfa2baf05349b49f9a08556e0593b8
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1استخلاصextracted with ether
- 2غسيلwashed with saturated aqueous NaCl
- 3تجفيفdried (MgSO4)
- 4أخرىevaporated
- 5أخرىto give a light yellow oil
الإجراء التجريبي
To a solution of isopropyl 1-(tert-butoxycarbonyl)pyrrolidin-5-one-2(S)-carboxylate (product of step 26B, 49.5 g, 183 mmol) in methanol (300 mL) was added sodium borohydride (10.0 g, 263 mmol) in ˜1 g portions over 1.5 hours. The reaction was stirred under nitrogen for another 10 minutes. It was diluted with water, extracted with ether, combined organic fractions washed with saturated aqueous NaCl, dried (MgSO4) and evaporated to give a light yellow oil. Flash chromatography (silica gel, 20-30% ethyl acetate/hexane) gave 31.8 g (64%) of isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate as a colorless syrup: 1H NMR (300 MHz, Chloroform-D) δ 5.16 (br d, 1 H, J=7.3 Hz), 5.03 (sept., 1 H, J=6.2 Hz), 4.28 (br d, 1 H, J=6.2 Hz), 3.67 (br dd, J=10.2, 5.5 Hz), 1.94-1.79 (m, 2 H), 1.76-1.67 (m, 1 H), 1.66-1.56 (m, 2 H), 1.43 (s, 9 H), 1.25 (d, 3 H, J=6.2 Hz), 1.23 (d, 3 H, J=6.2 Hz). LCMS m/z 276 (M+H)+.