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Hydrogen Peroxide → 6-(4-Phenylsulfinyl-butoxy)-3,4-dihydro-carbostyril

HRID 1065311
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1065311
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH2:6][CH2:5]2.C(=O)([O-])[O-].[K+].[K+].[C:19]1([S:25]([CH2:27][CH2:28][CH2:29][CH2:30]Br)=[O:26])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C1(S)C=CC=CC=1.BrCCCCBr.OO>CS(C)=O.C(O)(=O)C.O>[C:19]1([S:25]([CH2:27][CH2:28][CH2:29][CH2:30][O:1][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[NH:8][C:7](=[O:12])[CH2:6][CH2:5]3)=[O:26])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 6

HCID 784Hydrogen PeroxideHCID 7969ThiophenolHCID 80561,4-DibromobutaneHCID 11430Potassium CarbonateHCID 27740406-Hydroxy-3,4-dihydro-2(1H)-quinolinoneHCID 545301224-Phenylsulfinylbutylbromide

Produkt 1

HCID 13138341
6-(4-Phenylsulfinyl-butoxy)-3,4-dihydro-carbostyril

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 176Acetic AcidLösungsmittelHCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

32.6 gm (0.2 mol) of 6-hydroxy-3,4-dihydro-carbostyril [see F. F. Mayer et al., Ber. Dtsch. Chem. Ges. 60, 858 (1927)] and 27.6 gm (0.2 mol) of potassium carbonate were stirred for 5 minutes in 600 ml of dimethylsulfoxide which had been dried over a molecular sieve, and then 52.2 gm of 4-phenylsulfinyl-butyl bromide (0.2 mol) (prepared from thiophenol and 1,4-dibromo-butane and subsequent oxidation with hydrogen peroxide in glacial acetic acid analogous to Example 2; oily substance, solidified upon standing in the refrigerator) were added. After stirring it for 15 hours at 25° C., the reaction mixture was poured into 6 liters of water. After stirring the aqueous mixture for 30 minutes more, the precipitated product was suction-filtered off and thoroughly washed with water. After drying, the filter cake was recrystallized from about 600 ml of xylene in the presence of charcoal. White crystals with a melting point of 144.5°-145.5° C. were obtained.

Aufarbeitung

  1. customhad been dried over a molecular sieve
  2. additionwere added
  3. stirringAfter stirring the aqueous mixture for 30 minutes more
  4. filtrationthe precipitated product was suction-filtered off
  5. washthoroughly washed with water
  6. customAfter drying
  7. customthe filter cake was recrystallized from about 600 ml of xylene in the presence of charcoal
  8. customWhite crystals with a melting point of 144.5°-145.5° C. were obtained

Quellen und Nachweise

ORD-Eintrag
ord-813757f1bf554df4b45e6958d15c5ea1
Quelldatensatz
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04329347

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