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Water → Sodium 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfinate

HRID 2165038
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2165038
S([O-])([O-])=O.[Na+:5].[Na+].C(=O)([O-])O.[Na+].O.[C:13]([CH:18]([CH2:56][O:57][C:58]1[CH:63]=[CH:62][C:61]([C:64]([CH2:67][CH3:68])([CH3:66])[CH3:65])=[CH:60][CH:59]=1)[CH2:19][NH:20][C:21]([C:23]1[CH:24]=[C:25]([S:52](Cl)(=[O:54])=[O:53])[CH:26]=[C:27]([C:29](=[O:51])[NH:30][CH2:31][CH:32]([C:46]([CH2:49][CH3:50])([CH3:48])[CH3:47])[CH2:33][O:34][C:35]2[CH:40]=[CH:39][C:38]([C:41]([CH2:44][CH3:45])([CH3:43])[CH3:42])=[CH:37][CH:36]=2)[CH:28]=1)=[O:22])([CH2:16][CH3:17])([CH3:15])[CH3:14]>C(#N)C>[C:13]([CH:18]([CH2:56][O:57][C:58]1[CH:59]=[CH:60][C:61]([C:64]([CH2:67][CH3:68])([CH3:65])[CH3:66])=[CH:62][CH:63]=1)[CH2:19][NH:20][C:21]([C:23]1[CH:24]=[C:25]([S:52]([O-:54])=[O:53])[CH:26]=[C:27]([C:29](=[O:51])[NH:30][CH2:31][CH:32]([C:46]([CH2:49][CH3:50])([CH3:47])[CH3:48])[CH2:33][O:34][C:35]2[CH:40]=[CH:39][C:38]([C:41]([CH2:44][CH3:45])([CH3:43])[CH3:42])=[CH:37][CH:36]=2)[CH:28]=1)=[O:22])([CH2:16][CH3:17])([CH3:14])[CH3:15].[Na+:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 24437Sodium SulfiteHCID 516892Sodium BicarbonateHCID 867440573,5-Di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfonyl chloride

Produkt 1

HCID 67635903Sodium 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfinateAusbeute 82,8 %

Reagenzien, Katalysatoren, Lösungsmittel

1
HCID 6342AcetonitrileLösungsmittel2×

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

To 2 g (0.016 mol) of sodium sulfite and 2.4 g (0.029 mol) of sodium hydrogen carbonate were added 100 ml of water and 20 ml of acetonitrile and the mixture was stirred at 30° C. To the mixture was added dropwise a solution of 10.5 g (0.013 mol) of 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfonyl chloride obtained in the aforesaid step dissolved in 100 ml of acetonitrile. After stirring the resultant mixture for one hour, the reaction mixture was poured onto ice water and extracted with 150 ml of ethyl acetate. The ethyl acetate layer was washed thrice with cold water and dried over Glauber's salt. After filtrating away the Glauber's salt, the residue was concentrated to dryness to provide 8.6 g (yield of 82.8%) of a solid product.

Aufarbeitung

  1. customobtained in the aforesaid step
  2. additionthe reaction mixture was poured onto ice water
  3. extractionextracted with 150 ml of ethyl acetate
  4. washThe ethyl acetate layer was washed thrice with cold water
  5. dry with materialdried over Glauber's salt
  6. filtrationAfter filtrating away the Glauber's salt
  7. concentrationthe residue was concentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-a308812a977b490380459d687466991a
Quelldatensatz
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04939072

Notizen zur Reaktion

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