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HRID 233804Erstellt: 26. Oktober 2026

Methanesulfonic Acid → 2-Dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/233804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
EduktAmmonium HydroxideHCID 14923—
Edukt2-Dipropylamino-8-methylthio-1,2,3,4-tetrahydronaphthaleneHCID 9903735—
EduktSodium periodateHCID 23667635—
LösungsmittelWaterHCID 962—
Produkt2-Dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthaleneHCID 1904321085%

Reaktionsschritte

To a solution of water (60 mL) which contains methanesulfonic acid (0.16 mL, 2.33 mMol) was added 2-dipropylamino-8-methylthio-1,2,3,4-tetrahydronaphthalene (630 mg, 2.33 mMol). To this solution was added a solution of sodium metaperiodate (550 mg, 2.57 mMol) in water (10 mL), and the reaction mixture was stirred for two days at room temperature. The reaction mixture was made basic (NH4OH) and extracted with dichloromethane. The organic extracts were combined, dried (Na2SO4) and concentrated in vacuo to give the crude title compound as a light yellow oil. Purification by flash chromatography (3% methanol in dichloromethane+tr. NH4OH) gave the desired product (580 mg, 85%) as a colorless oil. The fumarate salt was formed. Recrystallization (ethanol/diethyl ether) gave a colorless, crystalline solid which was found to be extremely hygroscopic. Drying in a vacuum dessicator (60° C., 18 hours) gave a colorless glass (260 mg, m.p.=63° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594025
Quelldatensatzuspto-grants-1997_01
ORD IDord-95d28d1eddc741f6ad7cd7d5e514d86f
Quellennotizuspto-grants-1997_01