Formaldehyde → 929-53-3
Reaction equation
C=O.C(N[CH2:6][CH3:7])C.[CH2:8]1[CH2:12]O[CH2:10][CH2:9]1>>[CH:10]#[C:9][CH2:8][C:12]#[C:12][CH2:8][CH2:9][CH2:10][CH2:6][CH3:7]Participants
Procedure
19.5 G (0.65 mole) of paraformaldehyde, 54.8 g (0.75 mole) of diethylamine, 2.6 g of hydrated copper (II) acetate and 65 ml of THF were charged into a 1 l reactor. The mixture was maintained at reflux for 30 min and, still at reflux, the solution of deca-1,4-diyne obtained as described above was added thereto. The reaction mixture was kept at reflux for 11/2 h until the deca-1,4-diyne had completely disappeared. The mixture was then extracted at 0° with a 15% solution of HCl (3×70 ml) and the acidic layers were extracted with two fractions of 50 ml each of petroleum ether 80:100°, then 150 ml of a 30% NaOH solution were added thereto at 0°. The basic phase thus obtained was extracted with three fractions of 150 ml each of ethyl acetate and the organic extracts treated with a saturated aqueous solution of NaCl, dried over Na2SO4, filtered and evaporated to give 105 g of N,N-diethyl-undeca-2,5-diynyl-amine.
Workup
- temperatureThe mixture was maintained
- temperatureat reflux for 30 min
- temperaturestill at reflux
Sources & evidence
- ORD record
- ord-c641071360a34d009ef21b9dcffabe90
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300716
Reaction notes
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