تفاعل #1884985

ord-f05d44b4b66b43a09fe858518a084eb9

معادلة التفاعل

C=CCCCOC[C@H](NC(=O)OC(C)(C)C)C(=O)OC
N-tert-butoxycarbonyl-O-(4-pentenyl)-L-serine, methyl ester
O.[Li+].[OH-]
lithium hydroxide monohydrate
Cl
hydrochloric acid
C=CCCCOC[C@H](NC(=O)OC(C)(C)C)C(=O)O
N-tert-butoxycarbonyl-O-(4-pentenyl)-L-serine
المردود 100.2%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with water (3×) and brine
  2. 2
    تجفيفdried over anhydrous sodium sulfate
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated under vacuum

الإجراء التجريبي

To a solution of 6.65 g (23 mmol) of N-tert-butoxycarbonyl-O-(4-pentenyl)-L-serine, methyl ester in 500 mL of tetrahydrofuran at room temperature was added a solution of 1.95 g (46 mmol) of lithium hydroxide monohydrate in 100 mL of water. The resulting mixture was stirred at room temperature for 40 hours. To the reaction mixture then was added 46 mL of 1.00N hydrochloric acid. The mixture was diluted with ethyl acetate, washed with water (3×) and brine, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to afford 6.30 g of N-tert-butoxycarbonyl-O-(4-pentenyl)-L-serine as a colorless oil. NMR (300 MHz, CDCl3): δ 5.77 (d of d of t, 1 H, J=17.2, 10.2, 6.6 Hz), 5.37 (br d, 1 H, J=8.0 Hz), 5.03-4.92 (m, 2 H), 4.42 (m, 1 H), 3.87 (d of d, 1 H, J=9.5, 2.6 Hz), 3.63 (d of d, 1 H, J=9.5, 4.0 Hz), 3.45 (t, 2 H, J=6.6 Hz), 2.07 (quart., 2 H, J=7.3 Hz), 1.64 (quint., 2 H, J=7.3 Hz), 1.44 (s, 9 H).

المصدر

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