HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1,4,7,10Tetraaza-13-phosphatricyclo[5.5.1.04,13]tridecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Hexamethylphosphorous triamide | HCID 15355 | — |
| Reactant | 1,4,7,10-Tetraazacyclododecane | HCID 64963 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,4,7,10Tetraaza-13-phosphatricyclo[5.5.1.04,13]tridecane | HCID 53693611 | 100% |
Reaction Steps
A solution of 1.75 g of 1,4,7,10-tetraazacyclododecane and 1.63 g of hexamethylphosphorous triamide in 50 ml of toluene is refluxed for 12 hours. Titration of the off-gases with 1 N HCl indicates that 97% of the theoretical amount of dimethylamine is evolved in this time. The toluene is removed under reduced pressure to give 2.0 g of 1,4,7,10-tetraaza-13-phosphatricyclo[5.5.1.04,13 ]tridecane as a white solid which melts at 109°-111° C. with sintering from 90° C. (possibly because of the presence of a trace of toluene). Sublimation of this product at 75° C. and 0.55 mm gives large colorless crystals, which melt at 111°-113° C. The mass spectrum shows an M+ ion at 200; measured mass, 200.1194; calc'd, 200.1190.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04038312 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-31faa48ae3c84093aa13ea3a2dbd5c3c |
| Source note | uspto-grants-1977_07 |