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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683264Generated: October 30, 2026

Ammonium Hydroxide → 2-Di-n-propylamino-8-methylsulfonyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1683264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthaleneHCID 19043210—
SolventTrifluoroacetic acidHCID 6422—
Product2-Di-n-propylamino-8-methylsulfonyl-1,2,3,4-tetrahydronaphthaleneHCID 1904321130%

Reaction Steps

To a solution of 2-dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthalene (350 mg, 1.19 mMol) in trifluoroacetic acid (20 ml) was added a solution of metachloroperbenzoic acid (80%, 518 mg, 2.38 mMol) in trifluoroacetic acid (5 mL). The solution was stirred at room temperature for 18 hours and poured over ice. The resulting mixture was made basic (NH4OH) and extracted well with dichloromethane. The organic extracts were combined, dried (NA2SO4) and concentrated in vacuo to give the crude title compound as a brown oil. Purification by flash chromatography (3% methanol in dichloromethane+tr. NH4OH) gave the desired product as a light orange oil (110 mg, 30%). The maleate salt was formed. Recrystallization (ethanol/diethyl ether) gave a colorless solid (70 mg, m.p.=113°-114° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637624
Source datasetuspto-grants-1997_06
ORD IDord-f5c4a8de6e1f4bf7be7ce7467dff5b2c
Source noteuspto-grants-1997_06