Succinic anhydride → HCID 86624398, Verbindung

HRID 78689

Reaktionsgleichung

Reaktionsgleichung von HRID 78689
[SH:1][CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:9]1(=[O:15])[O:14][C:12](=[O:13])[CH2:11][CH2:10]1>CN(C1C=CN=CC=1)C.C(#N)C.N1C=CC=CC=1>[SH:1][CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:9]([OH:14])(=[O:15])[CH2:10][CH2:11][C:12]([OH:5])=[O:13]

Komponenten

5

Versuchsvorschrift

As shown in FIG. 2, Ethyl 3-mercaptopropionate (2.95 g, 22 mmol) was added under argon to a stirring solution of succinic anhydride (2.0 g, 20 mmol) and DMAP (122 mg, 1 mmol) in 25 ml of acetonitrile-pyridine (9:1). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and dried in vacuo. The residue was dissolved in 50 ml of EtOAc. The EtOAc solution was washed with 0.1 N HCl aqueous solution 30 ml×3, H2O×3, dried over anhydrous MgSO4. After filtration, the solution was concentrated to dry under reduced pressure and in vacuo. 1H NMR (CDCl3, 500 MHz) δ 10.23 (s, br), 4.14 (2H, q, J=7.0 Hz, —CH2—CH3), 3.13 (2H, t, J=7.0 Hz, —S—CH2—), 2.88 (2H, t, J=7.0 Hz, —S—CO—CH2—), 2.69 (2H, t, J=7.0 Hz, —S—CH2—CH2—), 2.62 (2H, t, J=7.0 Hz, —CH2—COOH), 1.25 (3H, t, J=7.0 Hz, —CH2—CH3).

Aufarbeitung

  1. concentrationThe solution was concentrated under reduced pressure
  2. customdried in vacuo
  3. dissolutionThe residue was dissolved in 50 ml of EtOAc
  4. washThe EtOAc solution was washed with 0.1 N HCl aqueous solution 30 ml×3, H2O×3
  5. dry with materialdried over anhydrous MgSO4
  6. filtrationAfter filtration
  7. concentrationthe solution was concentrated
  8. customto dry under reduced pressure and in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ba250d95f261483b8ef9cdf2da8c3578
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08841408B2

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