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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103339Generated: October 29, 2026

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

https://huagongshe.com/reaction/2103339

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 numberUS07576103B2
Source datasetuspto-grants-2009_08
ORD IDord-e8c421b83f2146429c497c91e678c94b
Source noteuspto-grants-2009_08