HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173696Generated: October 31, 2026
1-Methylimidazole → 3-[2-(Allyloxy)ethyl]-1-methylimidazolium bis(pentafluoroethyl)phosphinate
https://huagongshe.com/reaction/2173696
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | 2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinate | HCID 89782912 | — |
| Product | 3-[2-(Allyloxy)ethyl]-1-methylimidazolium bis(pentafluoroethyl)phosphinate | HCID 89782992 | — |
Reaction Steps
2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinate, (C2F5)2P(O)OCH2CH2—OCH2CH═CH2, (4.135 g; 10.7 mmol) is slowly added dropwise to dry and cooled (0° C.) N-methylimidazole (0.793 g; 9.7 mmol) (exothermic) in a 50 ml glass flask. A pale-yellow, more highly viscous solution forms spontaneously, which is stirred at 0° C. for 1.5 h, warmed and stirred at room temperature for 5 h. The readily volatile constituents are removed in vacuo (10−3 mbar) at room temperature. 3-[2-(Allyloxy)ethyl]-1-methylimidazolium bis(pentafluoroethyl)phosphinate, [CH2═CHCH2OCH2CH2MIM][(C2F5)2—P(O)O], (4.521 g; 9.7 mmol) is isolated as highly viscous, pale-yellow liquid in quantitative yield and a purity of 94%.
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-a17cb3ba23e94d55904f8d37e8539c67 |
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| Source note | uspto-grants-2015_06 |
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