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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072811Generated: October 28, 2026

Water → 1-[(Dimethylphosphinyl)methyl]-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/2072811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphine oxide, (chloromethyl)dimethyl-HCID 74224—
Reactant4-(2,3,4,5,6-Pentafluorophenoxy)piperidineHCID 14837040—
SolventDimethylformamideHCID 6228—
Product1-[(Dimethylphosphinyl)methyl]-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 1483706022.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring mixture of 9.0 g of potassium carbonate in 100 ml of dimethylformamide was added 8.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine and 9.5 g of dimethylphosphinylmethyl chloride. After stirring at 80° C. for 30 hours, the reaction mixture was cooled, poured into water, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, evaporation afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 5% methanol/dichloromethane). The desired fractions were evaporated to yield a solid which was sublimed to afford 2.37 g (22.1%) of 1-[(dimethylphosphinyl)methyl]-4-(2,3,4,5,6-pentafluorophenoxy) piperidine, m.p. 120°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914204
Source datasetuspto-grants-1990_04
ORD IDord-c8ae2803673e447999f1f12f21e73029
Source noteuspto-grants-1990_04