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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173694Generated: October 27, 2026

Ethylene glycol monoallyl ether → 2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinate

https://huagongshe.com/reaction/2173694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene glycol monoallyl etherHCID 8116—
ReactantPotassium FluorideHCID 522689—
Reactanttris(pentafluoroethyl)phosphine OxideHCID 11165593—
ReactantTris(pentafluoroethyl)phosphaneHCID 15809510—
Product2-(Allyloxy)ethyl bis(pentafluoroethyl)phosphinateHCID 8978291245%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium fluoride (0.277 g; 4.8 mmol) is suspended in tris(pentafluoro-ethyl)phosphine oxide, (C2F5)3P═O, (16.783 g; 41.5 mmol) in a 100 ml glass flask, cooled (0° C.), and 2-allyloxyethanol (4.188 g; 41.0 mmol) is added. The two-phase reaction suspension is stirred at 0° C. for 3 h and at room temperature for 20 h. After recondensation in vacuo (10−3 mbar) at 50° C. (decomposition is observed from 40° C.) and subsequent fractional distillation under reduced pressure (b.p.: 40 to 42° C. at 3.8·10−3 mbar), 2-(allyloxy)-ethyl bis(pentafluoroethyl)phosphinate, (C2F5)2P(O)OCH2CH2OCH2—CH═CH2, can be isolated as clear and colourless liquid (7.083 g; 18.3 mmol) in a yield of 45% and a purity of 96%. The product is stored at −20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056881B2
Source datasetuspto-grants-2015_06
ORD IDord-6104a8b2df844b938c994263409aeef7
Source noteuspto-grants-2015_06