Реакция #1747825

ord-f34b449409154d72bb3cc9b36b18d5b8

Уравнение реакции

C=CC1=CC(=O)CCC1
3-Vinyl-cyclohex-2-enone
CCCNCCC
dipropylamine
[Br-].[K+]
KBr
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
CCCN(CCC)CCC1=CC(=O)CCC1
3-(2-Dipropylamino-ethyl)-cyclohex-2-enone

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияfiltered
  2. 2
    Другоеevaporated to dryness
  3. 3
    Другоеwas destined in vacuo (175° C., 0.01 mm Hg)
  4. 4
    Другоеto give a slightly yellow oil which
  5. 5
    ДругоеRecrystallization from isopropyl ether/isopropyl alcohol
  6. 6
    Другоеyielded

Методика

3-Vinyl-cyclohex-2-enone (0.75 g, 6.1 mmol) (prepared according to Nasarow's method) was dissolved in acetonitril (1 mL) and dipropylamine (1.5 g, 16 mmol) was added followed by Cs2CO3 (50 mg). After stirring the mixture at rt for 3 h it was diluted with diethylether (100 mL), filtered and evaporated to dryness. The residue was destined in vacuo (175° C., 0.01 mm Hg) to give a slightly yellow oil which was converted to the hydrochloride salt. Recrystallization from isopropyl ether/isopropyl alcohol yielded: 1.2 g, 4.6 mmol (75%), mp 95-97° C. IR (KBr) 2962, 2613, 1667; 1H-NMR (CDCl3) δ 5.84 (d, 1H), 2.65 (m, 2H), 2.27-2.60 (m, 9H), 1.99 (m, 2H), 1.39-1.51 (m, 5H), 0.86 (t, 6H) ppm; 13C-NMR (CDCl3) δ 198.2, 163.5, 124.9, 54.2, 50.1, 35.7, 33.7, 28.4, 21.2, 18.5, 10.4 ppm; MS (EI) m/z 223 (M+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE042802E1uspto-grants-2011_10