HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Pentenoic acid → HCID 86636726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Pentenoic acid | HCID 61138 | — |
| Reactant | Dibutyl phosphate anion | HCID 3790919 | — |
| Reactant | HCID 86636727 | HCID 86636727 | — |
| Reactant | HCID 178443580 | HCID 178443580 | — |
| Product | HCID 86636726 | HCID 86636726 | — |
Reaction Steps
In a similar vein, hybrid dispersing agents were designed for CdSe nanoparticles and in this case, phosphine oxide chain ends were required for interaction with the surface of the CdSe. Using an anhydride functionalization approach requires 5-(dioctylphosphoryl)pentanoic anhydride, 13, which was synthesized by initial alkylation of di-n-butyl phosphate, 14, with octylmagnesium iodide followed by reaction with 4-pentenoic acid using AlBN to give 5-(dioctylphosphoryl)pentanoic acid, 15, which was converted into the desired anhydride, 13, using DCC (See FIG. 9). The anhydride was then used to functionalize the chain ends of 9a to give the phosphine oxide functionalized dendritic-linear copolymer, 16 (See FIG. 10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153729B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-957e702899d74f0b989b9243c2392d4a |
| Source note | uspto-grants-2012_04 |