Methanol → Tetracosa-11,13-diyne

HRID 1533843Notes

Reaction equation

HRID 1533843 reaction equation
[CH:1]#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].CO.CCO[CH2:18][CH3:19].O=O>N1C=CC=CC=1.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]#[C:12][C:1]#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:18][CH3:19]

Participants

7

Procedure

Dodec-1-yne (EGA 24,440-6) (1.2 g) was heated in the presence of copper acetate (4 g) in a mixture of pyridine (100 cm3) , methanol 300 cm3) and ether (400 cm3), for 72 h, at 30°-32° C., in the presence of a gentle stream of pure oxygen. The ether and methanol were then evaporated off under reduced pressure after the excess dissolved oxygen had been removed by the passage of argon, in the presence of 1 g of CuCl. The solution was taken up by fresh anhydrous pyridine (400 cm3) for 72 h at 47° C. (reflux). Part of the pyridine was then evaporated off under reduced pressure, after which the mixture was acidified with a 10% aqueous solution of HCl. After extraction with ether and evaporation, an oily liquid was obtained which crystallized in the cold. The oil was chromatographed in CHCl3 on SiO2 to give an oil which was transparent at room temperature (0.877 g, y=73%). The product was checked by NMR, gas chromatography (purity 97%) and mass spectroscopy (peak 330).

Workup

  1. customat 30°-32° C.
  2. customThe ether and methanol were then evaporated off under reduced pressure after the
  3. dissolutionexcess dissolved oxygen
  4. customhad been removed by the passage of argon, in the presence of 1 g of CuCl
  5. waitThe solution was taken up by fresh anhydrous pyridine (400 cm3) for 72 h at 47° C.
  6. temperature(reflux)
  7. customPart of the pyridine was then evaporated off under reduced pressure
  8. extractionAfter extraction
  9. customwith ether and evaporation
  10. customan oily liquid was obtained which
  11. customcrystallized in the cold
  12. customThe oil was chromatographed in CHCl3 on SiO2
  13. customto give an oil which
  14. customwas transparent at room temperature

Sources & evidence

ORD record
ord-deba32d1b1bd4c84b5b3274e9283ddc8
Source dataset
uspto-grants-1992_02
Patent number
US05085801

Reaction notes

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