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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715048Generated: October 31, 2026

Oxalyl chloride → 7-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

https://huagongshe.com/reaction/1715048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-[4-(Phenylsulfanyl)phenyl]butanoic acidHCID 24834548—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product7-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-oneHCID 5902173055.5%

Reaction Steps

4-(4-Phenylsulfanyl-phenyl)-butyric acid (5.0 g, 18.4 mmol) was dissolved in 50 mL tetrahydrofuran (THF). Oxalyl chloride (1.8 mL, 20 mmol) and one drop of DMF were added, and the reaction mixture was stirred for 1 hour, and then evaporated to dryness under reduced pressure. The resulting residue was dissolved in 40 mL of 1,2-dichloroethane, and aluminum trichloride (0.85 g, 25 mmol) was added all at once. The reaction mixture was stirred for 1 hour, and quenched by addition of 2% HCl. This aqueous mixture was extracted twice with 100 mL of EtOAc, and the combined organic layers were dried (MgSO4) and evaporated to yield 2.54 g (10 mmol, 55.5%) of 7-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one as a gummy residue. MS: 255 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799797B2
Source datasetuspto-grants-2010_09
ORD IDord-db1ab2347b0647cca4a6778d83f58895
Source noteuspto-grants-2010_09