HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256566Generated: October 27, 2026
Ammonium Hydroxide → 2-Di-n-propylamino-8-methylsulfonyl-1,2,3,4-tetrahydronaphthalene
https://huagongshe.com/reaction/256566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Dipropylamino-8-methylsulfinyl-1,2,3,4-tetrahydronaphthalene | HCID 19043210 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-Di-n-propylamino-8-methylsulfonyl-1,2,3,4-tetrahydronaphthalene | HCID 19043211 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258379 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-71ab2ec3e9934332a751187df33a6dc9 |
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| Source note | uspto-grants-1993_11 |
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