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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376961Erstellt: 26. Oktober 2026

1,3-Propanedithiol → 1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-one

https://huagongshe.com/reaction/376961

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-PropanedithiolHCID 8013—
EduktPotassium CarbonateHCID 11430—
Edukt2-Benzyl-2-(dimethylamino)-1-(4-fluorophenyl)butan-1-oneHCID 19360599—
LösungsmittelDimethylacetamideHCID 31374—
Produkt1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-oneHCID 19360633—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

32.5 g (0.3 mol) of 1,3-propanedithiol are dissolved in 50 ml of dry dimethylacetamide, and the solution is heated to about 50° C. together with 13.8 g (0.1 mol) of potassium carbonate. 15.0 g (0.05 mol) of 1-(4-fluorophenyl)-2-dimethylamino-2-benzyl-butan-1-one in 30 ml of dry dimethylacetamide are added dropwise. The suspension is stirred at 50° C. overnight (about 12 hours), then the solid is filtered off. The excess 1,3-propanedithiol and dimethylacetamide are distilled off. To the residue is added toluene, then the precipitate is filtered off. After distilling off the toluene, the residue is purified by means of column chromatography on silica gel with ethyl acetate-hexane (1:7) as an eluent, and an oily product is obtained. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm]: 0.68 (t, 3H), 1.39 (t, 1H), 1.79-1.88 (m, 1H), 1.97-2.11 (m, 3H), 2.36 (s, 6H), 2.69 (q, 2H), 3.12 (t, 2H), 3.19 (s, 2H), 7.15-7.27 (m, 7H), 8.28 (d, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06022906
Quelldatensatzuspto-grants-2000_02
ORD IDord-cab446e251fe4108813cf01645b94b33
Quellennotizuspto-grants-2000_02