HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625203Generated: October 25, 2026
Diphenyl Ether → Di-n-octylphosphinic acid
https://huagongshe.com/reaction/625203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | 1-Octadecene | HCID 8217 | — |
| Reactant | Trioctylphosphine oxide | HCID 65577 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Reactant | Oleylamine | HCID 5356789 | — |
| Reactant | Selenium | HCID 6326970 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Trioctylphosphine | HCID 20851 | — |
| Product | Di-n-octylphosphinic acid | HCID 99411 | — |
Reaction Steps
Materials. 1-methyl-2-pyrrolidinone (99.5%, Aldrich), 1-octadecene (90%, Aldrich), acetonitrile (99.9%, Fisher Chemical), BiCl3 (99.999%, Strem), CdO (99.5%, Aldrich), diphenyl ether (99%, Aldrich), methanol (ACS grade, VWR), oleic acid (90%, Aldrich), oleylamine (70% Aldrich), selenium (99.99%, Strem) trioctylphosphine (90%, Aldrich), trioctylphosphine oxide (99%, Strem), toluene (ACS grade, VWR). 1M TOP-Se was prepared by dissolving selenium powder in trioctylphosphine under inert atmosphere; trioctylphosphine oxide (TOPO) was recrystallized from acetonitrile prior to use; di-n-octylphosphinic acid (DOPA) was synthesized according to the procedure reported by Wang et. al.[1], a stock suspension of 2 mM BiCl3 in NMP was prepared in advance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09306110B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d148e86f3f324da9951be3659285ba16 |
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| Source note | uspto-grants-2016_04 |
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