Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 19956425 | HCID 19956425 | — |
| Product | HCID 19956435 | HCID 19956435 | — |
Reaction Steps
For conversion into the title compound, 37.45 g of crude (E)-1,14-di-allyl-1,5,10,14-tetra(diethoxyphosphoryl)-1,5,10,14-tetraazatetradec-7-ene are dissolved in 170 ml of 7THF, and hydrogen chloride is passed into the solution at 5° C. until saturated. The reaction mixture is stirred for 15 h at room temperature, 250 ml of diethyl ether are added to the resulting suspension, the mixture is filtered and the filtration residue is washed with a small amount of ethanol and diethyl ether. Recrystallisation from ethanol/water (with treatment with activated carbon) and drying the crystallisate under a high vacuum at 120° C. yield the title compound, m.p. >260° C. 1H-NMR (D2O): δ2.06-2.17(m,4H); 3.13-3.19(m,8H); 3.69(d,4H); 3.78(d,4H); 5.49-5.55(m,4H); 5.84-5.98(m,2H); 6.05-6.07(m,2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627215 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-73ac716fb9964bc5a8298300572d22fd |
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| Source note | uspto-grants-1997_05 |
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