Diisopropylamine → 1,1'-Dodecane-1,12-diyldicyclopropane carbonitrile

HRID 467992

Reaktionsgleichung

Reaktionsgleichung von HRID 467992
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].CCCCCC.[CH:12]([NH:15]C(C)C)(C)C.CN1C(=O)N(C)CCC1.[CH:28]1([C:31]#[N:32])[CH2:30][CH2:29]1.BrC[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45]Br>C1COCC1>[CH2:1]([C:28]1([C:31]#[N:32])[CH2:30][CH2:29]1)[CH2:2][CH2:3][CH2:4][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][C:37]1([C:12]#[N:15])[CH2:36][CH2:35]1

Komponenten

8

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

A solution of n-butyl lithium in hexane (1.8M, 1.06 L, 1.92 mol) was added drop wise to a solution of freshly distilled diisopropylamine (280.8 mL, 1.82 mol) in dry THF (1.5 L) at −60° C. under nitrogen atmosphere. The reaction mixture was slowly warmed to −20° C. and stirred for 30 min. The reaction mixture was re-cooled to −78° C., DMPU (29.3 g, 0.22 mol) was added drop wise and stirred for 15 min. Then cyclopropane carbonitrile (122.7 g, 1.82 mol) added drop wise over a period 1 h and stirred for 1 h. To the reaction mixture was added drop wise 1,12-dibromododecane (150.0 g, 0.45 mol) in dry THF (150 mL) and continued stirring at −78° C. for 2 h. The reaction mixture was slowly allowed to reach room temperature and continued stirring over a period of 16 h. The resulting reaction mixture was quenched with saturated NH4Cl (3.0 L) at 0° C. and the reaction mixture was extracted with ethyl acetate (1 L×3). The organic phases were combined, dried over anhydrous Na2SO4 and volatiles were evaporated under reduced pressure to yield a pale yellow liquid which was purified through silica gel (230-400) column (5% ethyl acetate in petroleum ether) to give product as off-white solid. The off-white solid washed with petroleum ether to obtain product as white solid 112 g (81.5%). mp: 45.0° C.-46.9° C.

Aufarbeitung

  1. temperatureThe reaction mixture was re-cooled to −78° C.
  2. stirringstirred for 15 min
  3. stirringstirred for 1 h
  4. stirringcontinued stirring at −78° C. for 2 h
  5. customto reach room temperature
  6. stirringcontinued stirring over a period of 16 h
  7. customThe resulting reaction mixture
  8. customwas quenched with saturated NH4Cl (3.0 L) at 0° C.
  9. extractionthe reaction mixture was extracted with ethyl acetate (1 L×3)
  10. dry with materialdried over anhydrous Na2SO4 and volatiles
  11. customwere evaporated under reduced pressure
  12. customto yield a pale yellow liquid which
  13. customwas purified through silica gel (230-400) column (5% ethyl acetate in petroleum ether)
  14. customto give product as off-white solid
  15. washThe off-white solid washed with petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-1288f2b84571425cb18f6bbc0a8dccc9
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08623897B2

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