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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphine oxide, (chloromethyl)dimethyl- | HCID 74224 | — |
| Reactant | 4-(2,3,4,5,6-Pentafluorophenoxy)piperidine | HCID 14837040 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(Dimethylphosphinyl)methyl]-4-(2,3,4,5,6-pentafluorophenoxy)piperidine | HCID 14837060 | 22.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04914204 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-c8ae2803673e447999f1f12f21e73029 |
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| Source note | uspto-grants-1990_04 |
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