반응 #2175446

ord-1495cf922ee14ef9ab2f1bcfd7edae27

반응 방정식

[N-]=[N+]=NCCOCCOCCOCCOCCOCCOCCOCCO
23-Azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol
CCN(CC)S(F)(F)F
DAST
[N-]=[N+]=NCCOCCOCCOCCOCCOCCOCCOCCF
4
수율 24.4%
[N-]=[N+]=NCCOCCOCCOCCOCCOCCOCCOCCF
23-azido-1-fluoro-3,6,9,12,15,18,21-heptaoxatricosane
수율 24.4%

용매

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to warm to room temperature
  2. 2
    workup.STIRRINGstirred for additional 20 hours
  3. 3
    기타The excess of DAST was quenched with methanol (5 mL)
  4. 4
    기타the solvents were subsequently evaporated at the reduced pressure
  5. 5
    workup.DISSOLUTIONThe oily residue was dissolved in the water (3 mL)
  6. 6
    기타The crude product was purified on semipreparative HPLC (System E)

실험 절차

23-Azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol (500 mg, 1.26 mmol) was dissolved in DCM (2 mL) and cooled to −10° C. DAST (482 μL, 3.78 mmol) was added in portions to the cooled solution and the resulting mixture was stirred at −10° C. for 30 minutes then allowed to warm to room temperature and stirred for additional 20 hours. The excess of DAST was quenched with methanol (5 mL) and the solvents were subsequently evaporated at the reduced pressure. The oily residue was dissolved in the water (3 mL) and the pH was adjusted to 5 using NaHCO3. The crude product was purified on semipreparative HPLC (System E) to yield 122 mg (24%) of 4 as a yellowish oil. 1H NMR (500 MHz, CDCl3): δ 3.39 (t, J=5.0 Hz, 2H), 3.65-3.68 (m, 26H), 3.75 (dt, J=4.2 Hz, 29.6 Hz, 2H), 4.56 (dt, J=4.0 Hz, 47.5 Hz, 2H); 13C NMR (125.7 MHz, CDCl3): δ 50.8, 70.1, 70.4, 70.5, 70.7-70.8, 70.9, 83.2 (d, J=169 Hz); 19F NMR (470.6 MHz, CDCl3): 6-225.9; MS ESI (m/z): [M+H]+ calcd. for C16H33FO7N3, 398.2; found 398.0.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08435488B2uspto-grants-2013_05