HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248867Generated: October 26, 2026
Formic Acid → 1-Formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine
https://huagongshe.com/reaction/248867
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | 4-(2,3,4,5,6-Pentafluorophenoxy)piperidine | HCID 14837040 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine | HCID 19762464 | 91% |
Reaction Steps
A mixture of 1.5 ml of formic acid and 3.5 ml of acetic anydride was stirred at 55° C. for one hour, cooled, and treated with a solution of 4.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine in 50 ml of diethyl ether. The reaction mixture was then stirred at ambient temperature for three hours. Thereafter, the mixture was poured into 100 ml of water, adjusted to pH 10 by the addition of sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated solution of chloride and dried over anhydrous magnesium sulfate. Filtration, followed by evaporation of the solvent afforded an oil which was purified by means of high pressure liquid chromatography (silica gel; elution with ethyl acetate) to yield 4.0 g (91%) of 1-formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine, m.p. 32°-34° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212184 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-de14a4d7a020427c9b58af4c229c58ca |
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| Source note | uspto-grants-1993_05 |
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