HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173695Generated: October 31, 2026
Pyridine → N-[2-(Allyloxy)ethyl]pyridinium bis(pentafluoroethyl)phosphinate
https://huagongshe.com/reaction/2173695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinate | HCID 89782912 | — |
| Product | N-[2-(Allyloxy)ethyl]pyridinium bis(pentafluoroethyl)phosphinate | HCID 89783222 | — |
Reaction Steps
2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinate, (C2F5)2P(O)O—CH2CH2OCH2CH═CH2, (2.407 g; 6.2 mmol) is slowly added dropwise to dry and cooled (0° C.) pyridine (0.502 g; 6.3 mmol) in a 25 ml glass flask. An orange, more highly viscous solution forms spontaneously, which is stirred at 0° C. for 1 h, warmed and stirred at room temperature for 2 h. The readily volatile constituents are removed in vacuo (10−3 mbar) at room temperature. N-[2-(Allyloxy)ethyl]pyridinium bis(pentafluoroethyl)phosphinate, [CH2═CHCH2OCH2CH2Py][(C2F5)2P(O)O], is isolated (2.829 g; 6.1 mmol) as highly viscous, intensely red-brown liquid in quantitative yield and a purity of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056881B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1f42b9354d774ea0b9264e224d341fc8 |
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| Source note | uspto-grants-2015_06 |
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