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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723619Generated: October 30, 2026

Acetic Acid → HCID 21877054, compound

https://huagongshe.com/reaction/723619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-HeptanedioneHCID 81923—
Reactant2,6-DifluorobenzaldehydeHCID 136284—
CatalystPiperidineHCID 8082—
SolventTolueneHCID 1140—
ProductHCID 21877054HCID 2187705430.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3,5-heptanedione (1.36 ml, 10 mmol), 2,6-difluorobenzaldehyde (1.08 ml, 10 mmol), piperidine (20 μL, 0.2 mmol), glacial acetic acid (149 μL, 2.6 mmol), molecular sieves and toluene (7 ml) was heated at 70° C., under a nitrogen atmosphere for 3 hours. Further 2,6-difluorobenzaldehyde (540 μL, 5 mmol) was added and the resulting mixture was stirred at 70° C. for a further 7 hours. After cooling, the molecular sieves were filtered off. The filtrate was concentrated under reduced pressure. The residue was partitioned between dichloromethane and water. The organic phase was dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel eluting with pentane:dichloromethane (4:1, by volume) and then with a solvent gradient of pentane:diethylether (20:1, by volume) gradually changing to pentane:diethylether (10:1, by volume) to afford the title compound (775 mg) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141585B2
Source datasetuspto-grants-2006_11
ORD IDord-889fc993a3e846d3bcdc91f48651226c
Source noteuspto-grants-2006_11