تفاعل #1884982

ord-e9bfa2baf05349b49f9a08556e0593b8

معادلة التفاعل

CC(C)OC(=O)[C@@H]1CCC(=O)N1C(=O)OC(C)(C)C
isopropyl 1-(tert-butoxycarbonyl)pyrrolidin-5-one-2(S)-carboxylate
[BH4-].[Na+]
sodium borohydride
CCCCCC.CCOC(C)=O
ethyl acetate hexane
CC(C)OC(=O)[C@H](CCCO)NC(=O)OC(C)(C)C
isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate
المردود 64.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ether
  2. 2
    غسيلwashed with saturated aqueous NaCl
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    أخرىevaporated
  5. 5
    أخرىto 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)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08343477B2uspto-grants-2013_01