HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104469Generated: October 31, 2026
1-Methylimidazole → HCID 178480871, compound
https://huagongshe.com/reaction/2104469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | 3,3,4,4,5,5,5-Heptafluoropentan-1-ol | HCID 2782534 | — |
| Reactant | tris(pentafluoroethyl)phosphine Oxide | HCID 11165593 | — |
| Reactant | Tris(pentafluoroethyl)phosphane | HCID 15809510 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178480871 | HCID 178480871 | 98.1% |
Reaction Steps
8.27 g (20.5 mmol) of tris(pentafluoroethyl)phosphine oxide, (C2F5)3P═O, are mixed with 20 cm3 of dry benzene and 1.67 g (20.3 mmol) of N-methylimidazole in a flask fitted with a reflux condenser held at minus 25° C. 4.37 g (20.4 mmol) of 3,3,4,4,5,5,5-heptafluoropentan-1-ol are added to this mixture at room temperature while stirring using a magnetic stirrer. The reaction mixture is heated at an oil-bath temperature of 100° C. for 20 minutes. After cooling to room temperature, the phosphinate is separated from the benzene phase and washed twice with 10 cm3 of benzene. Drying at 60° C. (2 hours) under a vacuum of 13.3 Pa gives 11.55 g of 1-(3,3,4,4,5,5,5-heptafluoropentyl)-3-methylimidazolium bis(pentafluoroethyl)phosphinate as liquid. The yield is 97.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576242B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-8649ed5baa454c67ad07a0505054ec10 |
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| Source note | uspto-grants-2009_08 |
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