HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → Hexakis(4-nitrophenoxy)cyclotriphosphazene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hexachlorocyclotriphosphazene | HCID 220225 | — |
| Product | Hexakis(4-nitrophenoxy)cyclotriphosphazene | HCID 272994 | — |
Reaction Steps
This material is prepared according to the method of Kober et al., Inorganic Chemistry, Vol. 5, p. 2239 (1966), which is incorporated herein by reference, by treatment of hexachlorocyclotriphosphazene with p-nitrophenol and potassium hydroxide. Hexakis(4-nitrophenoxy)-cyclotriphosphazene having a melting point of 261°-264° C. is obtained (lit. m.p. 264° C.). The infrared spectrum (in KBr), (cm-1) is 1589 (aromatic), 1522 and 1348 (asymmetrical and symmetrical nitro group stretching) and 1203, 1182 and 1163 (cyclotriphosphazene P=N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04668589 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-bae3662249dc4ab7a27eabf583804785 |
| Source note | uspto-grants-1987_05 |