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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824731Generated: November 1, 2026

Oxalyl chloride → HCID 66632440, compound

https://huagongshe.com/reaction/1824731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-Fluoro-1-naphthoic acidHCID 68448—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 21572690HCID 21572690—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66632440HCID 6663244098%

Reaction Conditions

Temperature4 °C

Reaction Steps

A stirred solution of 4-fluoro-1-naphthoic acid (0.5 g, 2.63 mmol) in anhydrous DCM (10 mL) is treated at room temperature with oxalyl chloride (0.52 g, 4.1 mmol) followed by a few drops of anhydrous DMF. Once bubbling subsided, the clear solution is cooled to 4° C. in an ice bath, and aluminium chloride (0.7 g, 5.25 mmol) is added in one portion. After stirring at 4° C. for 20 min, 1-pentyloxy-naphthalene (0.563 g, 2.63 mmol) is added, and the reaction mixture is allowed to warm gradually to ambient temperature overnight. The reaction mixture is distributed between ethyl acetate (50 mL) and water (250 mL) and extracted. The aqueous phase is additionally washed with fresh ethyl acetate (2×50 mL). The combined organic phases are dried (anhydrous MgSO4), filtered and concentrated in vacuo. The residue is purified by chromatography on silica gel using a Biotage apparatus (Dyax Corp.) and cyclohexane:ethyl acetate (9:1) as eluant to give the desired product (0.996 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045533B2
Source datasetuspto-grants-2006_05
ORD IDord-1c05776a1b32432d96b58995e1099935
Source noteuspto-grants-2006_05