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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080702Generated: October 26, 2026

1,2-Dichloroethane → 3,3,4,4,4-Pentafluorobutan-2-yl 4-formylbenzoate

https://huagongshe.com/reaction/2080702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHexaneHCID 8058—
Reactant4-Formylbenzoic acidHCID 12088—
Reactant3,3,4,4,4-Pentafluorobutan-2-olHCID 78991—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product3,3,4,4,4-Pentafluorobutan-2-yl 4-formylbenzoateHCID 5893072267%

Reaction Steps

A mixture of 4-carboxybenzaldehyde (21.9 g, 145.9 mmol), 3,3,4,4,4-pentafluoro-2-butanol (24.1 g, 146.9 mmol), EDC (33.5 g, 174.8 mmol) and DMAP (18.1 g, 148.1 mmol) was dissolved in DMF (60 ml) at rt. It was stirred for 36 h at rt. Hexane was added, it was washed with 1 N HCl, sat NaHCO3 and brine. The aqueous layers were extracted three times with hexane. It was dried over Na2SO4, filtered, concentrated, and the residue was purified by silica gel chromatography (ethyl acetate:hexane 1:10) to yield the desired aldehyde as a yellow oil (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932405B2
Source datasetuspto-grants-2011_04
ORD IDord-0e95271d66ec49f88794be995e20835b
Source noteuspto-grants-2011_04