Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620645Generated: October 31, 2026

Water → (3aR,6aS)-2-[2,4-bis(trifluoromethyl)phenyl]octahydrocyclopenta[c]pyrrole-5-carbaldehyde

https://huagongshe.com/reaction/1620645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2,4-bis(trifluoromethyl)benzeneHCID 20363895—
Reactant(3aR,6aS)-octahydrocyclopenta[c]pyrrol-5-ylmethanol hydrochlorideHCID 86678792—
SolventDimethylformamideHCID 6228—
Product(3aR,6aS)-2-[2,4-bis(trifluoromethyl)phenyl]octahydrocyclopenta[c]pyrrole-5-carbaldehydeHCID 8667881112.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (3aR,6aS)-octahydrocyclopenta[c]pyrrol-5-ylmethanol hydrochloride (862 mg) and potassium carbonate (1.68 g) in DMF (10 mL) was added 1-fluoro-2,4-bis(trifluoromethyl)benzene (1.24 g). The reaction mixture was stirred at 80° C. for 3 hr, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane). To a solution of the obtained oil (1.71 g) and triethylamine (2.03 mL) in DMSO (10 mL) and ethyl acetate (10 mL) was added sulfur trioxide pyridine complex (2.32 g) under cooling to 0° C. The reaction mixture was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (215 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-23eb1c9cecb7484ebf8932e1c1f64487
Source noteuspto-grants-2014_07