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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
Reactant4-(2,3,4,5,6-Pentafluorophenoxy)piperidineHCID 14837040—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 1976246491%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212184
Source datasetuspto-grants-1993_05
ORD IDord-de14a4d7a020427c9b58af4c229c58ca
Source noteuspto-grants-1993_05