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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613213Generated: October 30, 2026

Formic Acid → 1-Formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/1613213

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 sodium 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 numberUS05192776
Source datasetuspto-grants-1993_03
ORD IDord-1795bd04d0134526b5af4b293c120b4a
Source noteuspto-grants-1993_03