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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683263Generated: October 30, 2026

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

https://huagongshe.com/reaction/1683263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Dipropylamino-8-methylthio-1,2,3,4-tetrahydronaphthaleneHCID 9903735—
ReactantSodium periodateHCID 23667635—
SolventWaterHCID 962—
Product2-Dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthaleneHCID 1904321085%

Reaction Steps

To a solution of water (60 mL) which contains methanesulfonic acid (0.16 mL, 2.33 mMol) was added 2-di-propylamino-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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637624
Source datasetuspto-grants-1997_06
ORD IDord-6dd0b4e442a74b1897457ac276f883a7
Source noteuspto-grants-1997_06