Réaction #1755452

ord-d8f0833c4df84650b6f7e1855abc6ff0

Équation de réaction

CC(C)(C)OC(=O)CCCCCCCCCCBr
11-bromoundecanoic acid t-butyl ester
O=N[O-].[Na+]
NaNO2
Oc1cc(O)cc(O)c1
phloroglucinol
CC(C)(C)OC(=O)CCCCCCCCCC[N+](=O)[O-]
solid
Rendement 42.0%
CC(C)(C)OC(=O)CCCCCCCCCC[N+](=O)[O-]
11-Nitroundecanoic acid tert-butyl ester
Rendement 42.0%

Solvants

Conditions de réaction

Température
50°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter separation
  2. 2
    Extractionthe aqueous phase was further extracted with PET (3×30 mL)
  3. 3
    Séchagedried (Na2SO4)
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    AutreThe crude product was purified by silica-gel column chromatography (PET/diethyl ether 95/5)

Mode opératoire

In a 100 ml two-neck round bottom flask 11-bromoundecanoic acid t-butyl ester (6.10 g, 19.0 mmol) was dropped into a stirred solution of NaNO2 (2.60 g, 38.0 mmol) and phloroglucinol (3.10 g, 19.0 mmol) in DMF (10 ml). The reaction mixture was warmed at 50° C. and stirred for 24 h, then poured into a mixture of 40 mL of ice/water and 40 mL of PET. After separation, the aqueous phase was further extracted with PET (3×30 mL), dried (Na2SO4) and concentrated in vacuo. The crude product was purified by silica-gel column chromatography (PET/diethyl ether 95/5) obtaining a light yellow solid (2.29 g, 42%). M.p. 39-42° C. ESI-MS: 288 (MH+); (Calc. for C15H29NO4: 287 u.m.a.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07988950B2uspto-grants-2011_08