Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Product | 929-53-3 | HCID 11062440 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05300716 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-c641071360a34d009ef21b9dcffabe90 |
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| Source note | uspto-grants-1994_04 |
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