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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458309Generated: November 2, 2026

Hydrochloric Acid → N-(3-Fluoro-4-methyl-5-oxo-5,6,7,8-tetrahydro-1-naphthyl)acetamide

https://huagongshe.com/reaction/1458309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropyl EtherHCID 7914—
ReactantThionyl ChlorideHCID 24386—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-(2-Acetamido-4-fluoro-5-methylphenyl)butanoic acidHCID 22444950—
SolventDichloromethaneHCID 6344—
ProductN-(3-Fluoro-4-methyl-5-oxo-5,6,7,8-tetrahydro-1-naphthyl)acetamideHCID 2210195475.4%

Reaction Steps

In 50 ml of methylene chloride, 5.0 g of 4-(2 -acetylamino-4-fluoro-5-methylphenyl)butanoic acid was suspended. To the suspension, 4.3 ml of thionyl chloride was added dropwise over 2 minutes at an internal temperature of 3° to 4° C., followed by stirring at the same temperature for 15 minutes and then at room temperature for 45 minutes. To the resulting mixture, 6.6 g of aluminum chloride were added over 5 minutes at an internal temperature of 4° to 6° C., followed by stirring for one hour at the same temperature and then stirring for 24 hours at room temperature. After the completion of the reaction, a 5% aqueous hydrochloric acid solution and ice were added gradually to the reaction mixture and they were stirred for a while. The reaction mixture was extracted with chloroform. The chloroform layer was washed sufficiently with water and a saturated aqueous solution of sodium bicarbonate, and was then dried over potassium carbonate. The solvent was removed under reduced pressure. To the residue so obtained, isopropyl ether was added. The crystals so precipitated were collected by filtration, whereby 3.5 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849945
Source datasetuspto-grants-1998_12
ORD IDord-3f9db8c4cca04839b8b1e229ee5eac3d
Source noteuspto-grants-1998_12